On 11/05/2025, SUN PHARMACEUTICAL recalled LISDEXAMFETAMINE DIMESYLATE 70 MG due to Failed Dissolution Specifications: An out of specification results observed in dissolution test during analysis at 12-month long term stability station (25°C, 60%RH) for Lisdexamfetamine dimesylate capsules. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: LISDEXAMFETAMINE DIMESYLATE70 MG
NDC Number: 57664005288
Lot Number(s): AD48712, AD50898
Expiration Date(s): 04/30/2026, 05/31/2026

What you should do:

• Check your prescription label to see if you have any LISDEXAMFETAMINE DIMESYLATE in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 11/05/2025, SUN PHARMACEUTICAL recalled LISDEXAMFETAMINE DIMESYLATE 50 MG due to Failed Dissolution Specifications: An out of specification results observed in dissolution test during analysis at 12-month long term stability station (25°C, 60%RH) for Lisdexamfetamine dimesylate capsules. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: LISDEXAMFETAMINE DIMESYLATE50 MG
NDC Number: 57664005088
Lot Number(s): AD48710, AD50895
Expiration Date(s): 04/30/2026, 05/31/2026

What you should do:

• Check your prescription label to see if you have any LISDEXAMFETAMINE DIMESYLATE in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178. 

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 11/05/2025, SUN PHARMACEUTICAL recalled LISDEXAMFETAMINE DIMESYLATE 40 MG due to Failed Dissolution Specifications: An out of specification results observed in dissolution test during analysis at 12-month long term stability station (25°C, 60%RH) for Lisdexamfetamine dimesylate capsules. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: LISDEXAMFETAMINE DIMESYLATE40 MG
NDC Number: 57664004988
Lot Number(s): AD48709, AD50894
Expiration Date(s): 04/30/2026, 05/31/2026

What you should do:

• Check your prescription label to see if you have any LISDEXAMFETAMINE DIMESYLATE in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 11/05/2025, SUN PHARMACEUTICAL recalled LISDEXAMFETAMINE DIMESYLATE 30 MG due to Failed Dissolution Specifications: An out of specification results observed in dissolution test during analysis at 12-month long term stability station (25°C, 60%RH) for Lisdexamfetamine dimesylate capsules. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: LISDEXAMFETAMINE DIMESYLATE30 MG
NDC Number: 57664004888
Lot Number(s): AD42470, AD48708
Expiration Date(s): 02/28/2026, 04/30/2026

What you should do:

• Check your prescription label to see if you have any LISDEXAMFETAMINE DIMESYLATE in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 11/05/2025, SUN PHARMACEUTICAL recalled LISDEXAMFETAMINE DIMESYLATE 20 MG due to Failed Dissolution Specifications: An out of specification results observed in dissolution test during analysis at 12-month long term stability station (25°C, 60%RH) for Lisdexamfetamine dimesylate capsules. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: LISDEXAMFETAMINE DIMESYLATE20 MG
NDC Number: 57664004788
Lot Number(s): AD42469, AD48707
Expiration Date(s): 02/28/2026, 04/30/2026

What you should do:

• Check your prescription label to see if you have any LISDEXAMFETAMINE DIMESYLATE in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 11/05/2025, BRECKENRIDGE recalled DULOXETINE HCL 60 MG due to CGMP Deviations: N-nitroso-duloxetine impurity above the safety assessment limit of 12.5ppm. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the
affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: DULOXETINE HCL60 MG
NDC Number: 51991074890, 51991074810
Lot Number(s): 240721C, 230286C
Expiration Date(s): 02/28/2027, 02/28/2026

What you should do:

• Check your prescription label to see if you have any DULOXETINE HCL in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 11/05/2025, TEVA USA recalled PRAZOSIN HCL 1 MG due to CGMP Deviations-Test results for N-nitroso Prazosin impurity C that are above the Carcinogenic Potency Categorization Approach (CPCA) acceptable intake limit for the above specified lots.

The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: PRAZOSIN HCL1 MG
NDC Number: 00093406701
Lot Number(s): 3010544A, 3010545A, 3010567A, 3010590A, 3010601A, 3010602A, 3010603A, 3010652A, 3010670A, 3010671A, 3010678A, 3010700A, 3010701A, 3010440A, 3010672A
Expiration Date(s): 10/2025, 10/2025, 12/2025, 02/2026, 03/2026, 03/2026, 03/2026, 07/2026, 07/2026, 07/2026, 08/2026, 08/2026, 08/2026, 12/2025, 07/2026

What you should do:

• Check your prescription label to see if you have any PRAZOSIN HCL in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 11/05/2025, TEVA USA recalled PRAZOSIN HCL 2 MG due to CGMP Deviations-est results for N-nitroso Prazosin impurity C that are above the Carcinogenic Potency Categorization Approach (CPCA) acceptable intake limit for the above specified lots.

The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: PRAZOSIN HCL2 MG
NDC Number: 00093406801, 00093406810
Lot Number(s): 3010398A, 3010399A, 3010400A, 3010401A, 3010353A, 3010439A, 3010388A, 3010526A, 3010527A, 3010591A, 3010343A, 3010352A, 3010468A, 3010469A, 3010461A, 3010629A, 3010653A, 3010654A, 3010679A, 3010702A, 3010547A, 3010402A, 3010593A, 3010610A
Expiration Date(s): 12/2025, 12/2025, 12/2025, 12/2025, 12/2025, 01/2026, 01/2026, 03/2026, 03/2026, 07/2026, 10/2025, 11/2025, 02/2026, 02/2026, 02/2026, 09/2026, 01/2027, 02/2027, 02/2027, 02/2027, 04/2026, 02/2028, 07/2026, 09/2026

What you should do:

• Check your prescription label to see if you have any PRAZOSIN HCL in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 11/05/2025, TEVA USA recalled PRAZOSIN HCL 5 MG due to CGMP Deviations-Test results for N-nitroso Prazosin impurity C that are above the Carcinogenic Potency Categorization Approach (CPCA) acceptable intake limit for the above specified lots.

The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: PRAZOSIN HCL5 MG
NDC Number: 00093406901, 00093406952, 00093406905
Lot Number(s): 3010403A, 3010385A, 3010404A, 3010405A, 3010510A, 3010528A, 3010354A, 3010592A, 3010605A, 3010611A, 3010612A, 3010655A, 3010703A, 3010430A, 3010613A, 3010406A
Expiration Date(s): 02/2026, 02/2026, 02/2026, 03/2026, 03/2026, 03/2026, 03/2026, 08/2026, 08/2026, 08/2026, 08/2026, 02/2027, 02/2027, 11/2025, 08/2026, 02/2026

What you should do:

• Check your prescription label to see if you have any PRAZOSIN HCL in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 10/29/2025, GRAVITI PHARMACEUTICALS recalled BUPROPION XL 300 MG due to Failed Tablet/Capsule Specifications. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: BUPROPION XL300 MG
NDC Number: 16571086303
Lot Number(s): BPB124341A
Expiration Date(s): 10/2026

What you should do:

• Check your prescription label to see if you have any BUPROPION XL in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 10/15/2025, ACCORD HEALTHCARE recalled LEVOTHYROXINE SODIUM 88 MCG due to Subpotent: During long term stability testing of Levothyroxine Sodium Tablets USP for 88 mcg, the assay content was observed below the approved specification range. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: LEVOTHYROXINE SODIUM88 MCG
NDC Number: 16729045015
Lot Number(s): D2300045
Expiration Date(s): 12/31/2025

What you should do:

• Check your prescription label to see if you have any LEVOTHYROXINE SODIUM in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 10/08/2025, APOTEX CORP recalled KETOROLAC TROMETHAMINE 0.5 % due to Lack of Assurance of Sterility; atypical weight loss due to improper bottle sealing leading to potential sterility concerns. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: KETOROLAC TROMETHAMINE0.5 %
NDC Number: 60505100301
Lot Number(s): VA0444, VA4608 and TZ7016
Expiration Date(s): 01/2026, 01/2026 and 12/2025

What you should do:

• Check your prescription label to see if you have any KETOROLAC TROMETHAMINE in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178. 

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 09/24/2025, ASCEND LABORATORIES LLC recalled ARIPIPRAZOLE 10 MG due to superpotent drug. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: ARIPIPRAZOLE10 MG
NDC Number: 67877043203
Lot Number(s): 24144162
Expiration Date(s): 09/2027

What you should do:

• Check your prescription label to see if you have any ARIPIPRAZOLE in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 08/13/2025, ALEMBIC PHARMACEUTICALS recalled DOXEPIN HCL 10 MG due to CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity above the proposed interim limit. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: DOXEPIN HCL10 MG
NDC Number: 62332063731
Lot Number(s): 2305015142
Expiration Date(s): 09/30/2025

What you should do:

• Check your prescription label to see if you have any DOXEPIN HCL in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 08/13/2025, SUN PHARMACEUTICALS recalled SPIRONOLACTONE 25 MG due to the Presence of foreign substance: identified as aluminum. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: SPIRONOLACTONE25 MG
NDC Number: 53489014301
Lot Number(s): P3314
Expiration Date(s): 11/30/2026

What you should do:

• Check your prescription label to see if you have any SPIRONOLACTONE in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 08/06/2025, NOSTRUM LABORATORIES recalled SUCRALFATE 1 G due to CGMP Deviations: The recalling firm filed for Chapter 11 in September 2024. As a result, it cannot monitor the quality program and hence cannot assure that products meet the identity, strength, quality, and purity characteristics that they are purported or represented to possess, rendering the products adulterated. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: SUCRALFATE1 G
NDC Number: 29033000305
Lot Number(s): All Lots
Expiration Date(s): All Expiration Dates

What you should do:

• Check your prescription label to see if you have any SUCRALFATE in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 07/23/2025, ACCORD HEALTHCARE recalled LEVOTHYROXINE SODIUM 100 MCG due to Subpotent Drug: Assay below the approved specification. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: LEVOTHYROXINE SODIUM 100 MCG
NDC Number: 16729045117
Lot Number(s): D2300092, D2400722
Expiration Date(s): 12/31/2025, 03/31/2026

What you should do:

• Check your prescription label to see if you have any LEVOTHYROXINE SODIUM in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 07/23/2025, ACCORD HEALTHCARE recalled LEVOTHYROXINE SODIUM 112 MCG due to Subpotent Drug: Assay below the approved specification. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected
medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: LEVOTHYROXINE SODIUM 112 MCG
NDC Number: 16729045217
Lot Number(s): D2300104
Expiration Date(s): 12/31/2025

What you should do:

• Check your prescription label to see if you have any LEVOTHYROXINE SODIUM in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 07/23/2025, ACCORD HEALTHCARE recalled LEVOTHYROXINE SODIUM 150 MCG due to Subpotent Drug: Assay below the approved specification. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected
medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: LEVOTHYROXINE SODIUM 150 MCG
NDC Number: 16729045517
Lot Number(s): D2300076
Expiration Date(s): 12/31/2025

What you should do:

• Check your prescription label to see if you have any LEVOTHYROXINE SODIUM in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 07/23/2025, ACCORD HEALTHCARE recalled LEVOTHYROXINE SODIUM 175 MCG due to Subpotent Drug: Assay below the approved specification. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected
medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: LEVOTHYROXINE SODIUM 175 MCG
NDC Number: 16729045617
Lot Number(s): D2300042
Expiration Date(s): 12/31/2025

What you should do: 

• Check your prescription label to see if you have any LEVOTHYROXINE SODIUM in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 07/23/2025, ACCORD HEALTHCARE recalled LEVOTHYROXINE SODIUM 25 MCG due to Subpotent Drug: Assay below the approved specification. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected
medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: LEVOTHYROXINE SODIUM 25 MCG
NDC Number: 16729044715
Lot Number(s): D2300325, D2400536
Expiration Date(s): 01/31/2026, 02/28/2026

What you should do:

• Check your prescription label to see if you have any LEVOTHYROXINE SODIUM in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 07/23/2025, ACCORD HEALTHCARE recalled LEVOTHYROXINE SODIUM 25 MCG due to Subpotent Drug: Assay below the approved specification. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected
medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: LEVOTHYROXINE SODIUM 25 MCG
NDC Number: 16729044717
Lot Number(s): D2400679
Expiration Date(s): 02/28/2026

What you should do:

• Check your prescription label to see if you have any LEVOTHYROXINE SODIUM in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 07/23/2025, ACCORD HEALTHCARE recalled LEVOTHYROXINE SODIUM 50 MCG due to Subpotent Drug: Assay below the approved specification. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected
medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: LEVOTHYROXINE SODIUM 50 MCG
NDC Number: 16729044815
Lot Number(s): D2300087
Expiration Date(s): 12/31/2025

What you should do:

•  Check your prescription label to see if you have any LEVOTHYROXINE SODIUM in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 07/09/2025, GRANULES PHARMA recalled METOPROLOL SUCCINATE 25 MG due to Failed Dissolution Specifications: Product failed to meet dissolution acceptance criteria in the stability studies at the 6th month (25¿C/60% RH) long-term. The U.S.

Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: METOPROLOL SUCCINATE25 MG
NDC Number: 70010078001
Lot Number(s): 1400008A
Expiration Date(s): 12/31/2025

What you should do:

• Check your prescription label to see if you have any METOPROLOL SUCCINATE in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 07/09/2025, GRANULES PHARMA recalled METOPROLOL SUCCINATE 25 MG due to Failed Dissolution Specifications: Product failed to meet dissolution acceptance criteria in the stability studies at the 6th month (25¿C/60% RH) long-term. The U.S.

Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: METOPROLOL SUCCINATE25 MG
NDC Number: 70010078005
Lot Number(s): 1400008B
Expiration Date(s): 12/31/2025

What you should do:

• Check your prescription label to see if you have any METOPROLOL SUCCINATE in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 07/02/2025, TEVA PHARMACEUTICALS recalled METOCLOPRAMIDE HCL 10 MG due to the Presence of foreign tablets/capsules. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: METOCLOPRAMIDE HCL10 MG
NDC Number: 00093220301
Lot Number(s): 5420094
Expiration Date(s): 09/30/2027

What you should do:

• Check your prescription label to see if you have any METOCLOPRAMIDE HCL in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 07/02/2025, APOTEX CORP recalled KETOROLAC TROMETHAMINE 0.5 % due to Lack of Assurance of Sterility. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: KETOROLAC TROMETHAMINE0.5 %
NDC Number: 60505100302
Lot Number(s): TZ1236
Expiration Date(s): 11/30/2025

What you should do:

• Check your prescription label to see if you have any KETOROLAC TROMETHAMINE in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 07/02/2025, APOTEX CORP recalled AZELASTINE HCL 0.05 % due to Lack of Assurance of Sterility. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: AZELASTINE HCL0.05 %
NDC Number: 60505057804
Lot Number(s): VD1654
Expiration Date(s): 06/30/2027

What you should do:

• Check your prescription label to see if you have any AZELASTINE HCL in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 06/04/2025, GLENMARK PHARMACEUTICALS recalled CARVEDILOL 6.25 MG due to CGMP Deviations; presence ‘N-Nitroso Carvedilol I’ Impurity above the recommended acceptable intake limit. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: CARVEDILOL6.25 MG
NDC Number: 68462016305
Lot Number(s): 19231174, 19231199, 19231164, 19231517,19231527, 19231566, 19231568, 19231595, 19231618, 19231634, 19231638, 19231448, 19232043, 19232051, 19232064, 19232322, 19232324, 19232365, 19232380, 19232389, 19232736, 19232743, 19232746, 19232756, 19232757, 19233369, 19233371, 19233405, 19233416, 19234162, 19234183, 19234192, 19234204, 19234223, 19234243, 19234263, 19234165, 19234242, 19234743, 19234774, 19234993, 19240223, 19240203, 19240211, 19240214, 19240247, 19240249, 19240272, 19240319 and 19240543
Expiration Date(s): Feb-25, Mar-25, Apr-25, May-25, Jun-25, Jul-25, Sep-25, Nov-25, Dec-25 and Jan-26

What you should do:

• Check your prescription label to see if you have any CARVEDILOL in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

On 06/04/2025, GLENMARK PHARMACEUTICALS recalled CARVEDILOL 6.25 MG due to CGMP Deviations; presence ‘N-Nitroso Carvedilol I’ Impurity above the recommended acceptable intake limit. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: CARVEDILOL6.25 MG
NDC Number: 68462016301
Lot Number(s): 19233369, 19234162 and 19240543
Expiration Date(s): Jul-25, Sep-25, and Jan-26

What you should do:

• Check your prescription label to see if you have any CARVEDILOL in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 06/04/2025, GLENMARK PHARMACEUTICALS recalled CARVEDILOL 3.125 MG due to CGMP Deviations; presence ‘N-Nitroso Carvedilol I’ Impurity above the recommended acceptable intake limit. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: CARVEDILOL3.125 MG
NDC Number: 68462016205
Lot Number(s): 19231450, 19231464, 19231471, 19231493, 19232083, 19232103, 19232658, 19233328, 19233343, 19233344, 19233345, 19234275,19234843, 19235039, 19240280 and 19240296
Expiration Date(s): Mar-25, Apr-25, Jun-25, Jul-25, Sep-25, Nov-25 and Dec-25

What you should do:

• Check your prescription label to see if you have any CARVEDILOL in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 06/04/2025, GLENMARK PHARMACEUTICALS recalled CARVEDILOL 3.125 MG due to CGMP Deviations; presence ‘N-Nitroso Carvedilol I’ Impurity above the recommended acceptable intake limit. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: CARVEDILOL3.125 MG
NDC Number: 68462016201
Lot Number(s): 19231450, 19233345, 19234275 and 19240280
Expiration Date(s): Mar-25, Jul-25, Sep-25 and Dec-25

What you should do:

• Check your prescription label to see if you have any CARVEDILOL in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 06/04/2025, GLENMARK PHARMACEUTICALS recalled CARVEDILOL 25 MG due to CGMP Deviations; presence ‘N-Nitroso Carvedilol I’ Impurity above the recommended acceptable intake limit. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: CARVEDILOL25 MG
NDC Number: 68462016505
Lot Number(s): 19231107, 19231114, 19231152 and 19234866
Expiration Date(s): Feb-25 and Jan-26

What you should do:

• Check your prescription label to see if you have any CARVEDILOL in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 06/04/2025, GLENMARK PHARMACEUTICALS recalled CARVEDILOL 12.5 MG due to CGMP Deviations; presence ‘N-Nitroso Carvedilol I’ Impurity above the recommended acceptable intake limit. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: CARVEDILOL12.5 MG
NDC Number: 68462016405
Lot Number(s): 19231899, 19231922, 19231927, 19231967, 19231979, 19232226, 19232234, 19232265, 1923227,19232758, 19232759, 19232762 and 19232788
Expiration Date(s): Apr-25, May-25 and Jun-25

What you should do:

• Check your prescription label to see if you have any CARVEDILOL in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 05/07/2025, ACCORD HEALTHCARE recalled LEVOTHYROXINE SODIUM 112 MCG due to Subpotent Drug. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: LEVOTHYROXINE SODIUM 112 MCG
NDC Number: 16729045215
Lot Number(s): D2400725
Expiration Date(s): 03/2026

What you should do:

• Check your prescription label to see if you have any LEVOTHYROXINE SODIUM in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 05/07/2025, ACCORD HEALTHCARE recalled LEVOTHYROXINE SODIUM 88 MCG due to Subpotent Drug. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: LEVOTHYROXINE SODIUM 88 MCG
NDC Number: 16729045017
Lot Number(s): D2300044
Expiration Date(s): 12/2025

What you should do:

• Check your prescription label to see if you have any LEVOTHYROXINE SODIUM in the affected lot numbers and expiration dates. 
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 05/07/2025, ACCORD HEALTHCARE recalled LEVOTHYROXINE SODIUM 50 MCG due to Subpotent Drug. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: LEVOTHYROXINE SODIUM 50 MCG
NDC Number: 16729044817
Lot Number(s): D2400547
Expiration Date(s): 02/2026

What you should do:

• Check your prescription label to see if you have any LEVOTHYROXINE SODIUM in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 05/07/2025, ACCORD HEALTHCARE recalled LEVOTHYROXINE SODIUM 25 MCG due to Subpotent Drug. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: LEVOTHYROXINE SODIUM 25 MCG
NDC Number: 16729044717
Lot Number(s): D2300323
Expiration Date(s): 01/2026

What you should do:

• Check your prescription label to see if you have any LEVOTHYROXINE SODIUM in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 04/23/2025, EUGIA US LLC recalled TESTOSTERONE CYPIONATE 200 MG/ML due to cGMP: complaints of crystals not redissolving into solution after warming and shaking the vials. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: TESTOSTERONE CYPIONATE200 MG/ML
NDC Number: 55150027701
Lot Number(s): 1TC24075A
Expiration Date(s): 11/30/2026

What you should do:

• Check your prescription label to see if you have any TESTOSTERONE CYPIONATE in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178. 

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 04/16/2025, GLENMARK PHARMACEUTICALS recalled CARVEDILOL 12.5 MG due to CGMP Deviations. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: CARVEDILOL 12.5 MG
NDC Number: 68462016405
Lot Number(s): 17240238, 17240243, 17240245 and 17240248
Expiration Date(s): Jan-26, Jan-26, Jan-26 and Jan-26

What you should do:

• Check your prescription label to see if you have any CARVEDILOL in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 04/16/2025, GLENMARK PHARMACEUTICALS recalled FENOFIBRATE 67 MG due to CGMP Deviations. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: FENOFIBRATE 67 MG
NDC Number: 68462058001
Lot Number(s): 17230834 and 17230835
Expiration Date(s): Mar-25 and Mar-25

What you should do:

• Check your prescription label to see if you have any FENOFIBRATE in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 04/16/2025, GLENMARK PHARMACEUTICALS recalled GABAPENTIN 600 MG due to CGMP Deviations. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: GABAPENTIN 600 MG
NDC Number: 68462012605
Lot Number(s): 17231015, 17231128, 17231138, 17231139, 17231143, 17231144, 17231848, 17231898, 17231977, 17231978, 17232015, 17232016, 17232017, 17232034, 17232041, 17232396, 17232406, 17232410, 17232490, 17240326, 17240327, 17240383, 17240395, 17241863, 17241869, 17241870, 17231256, 17231386, 17231387, 17231407, 17231417, 17231418, 17231754, 17240085, 17240117 and 17240131
Expiration Date(s): Apr-25, Apr-25, Apr-25, Apr-25, Apr-25, Apr-25, Aug-25, Aug-25, Aug-25, Aug-25, Aug-25, Aug-25, Aug-25, Aug-25, Aug-25, Nov-25, Nov-25, Nov-25, Nov-25, Jan-26, Jan-26, Feb-26, Feb-26, Oct-26, Oct-26, Oct-26, May-25, May-25, May-25, May-25, May-25, May-25, May-25, Jul-25, Dec-25 and Dec-25

What you should do:

• Check your prescription label to see if you have any GABAPENTIN in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 04/16/2025, GLENMARK PHARMACEUTICALS recalled LACOSAMIDE 100 MG due to CGMP Deviations. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: LACOSAMIDE 100 MG
NDC Number: 68462067960
Lot Number(s): 17232533, 17232534, 17240606, 17240619, 17240911, 17240912, 17241121 and 17241124
Expiration Date(s): Nov-25, Nov-25, Mar-26, Mar-26, May-26, May-26, Jun-26 and Jun-26

What you should do:

• Check your prescription label to see if you have any LACOSAMIDE in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 04/16/2025, GLENMARK PHARMACEUTICALS recalled NAPROXEN SODIUM 550 MG due to CGMP Deviations. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: NAPROXEN SODIUM 550 MG
NDC Number: 68462017901
Lot Number(s): 17231956
Expiration Date(s): Aug-25

What you should do:

• Check your prescription label to see if you have any NAPROXEN SODIUM in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 04/16/2025, GLENMARK PHARMACEUTICALS recalled DILTIAZEM 12HR ER 120 MG due to CGMP Deviations. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: DILTIAZEM 12HR ER 120 MG
NDC Number: 68462056201
Lot Number(s): 17241067 and 17241628
Expiration Date(s): May-26 and Aug-26

What you should do:

• Check your prescription label to see if you have any DILTIAZEM in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 04/16/2025, GLENMARK PHARMACEUTICALS recalled NITROGLYCERIN 0.4 MG due to CGMP Deviations. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: NITROGLYCERIN 0.4 MG
NDC Number: 68462063945
Lot Number(s): 17232024, 17232071 and 17232072
Expiration Date(s): Aug-25, Sep-25 and Sep-25

What you should do:

• Check your prescription label to see if you have any NITROGLYCERIN in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 04/16/2025, NORTHSTAR RX LLC recalled PRAVASTATIN SODIUM 80 MG due to CGMP Deviations. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: PRAVASTATIN SODIUM 80 MG
NDC Number: 16714057001
Lot Number(s): 17221770, 17221774, 17231251, 17231262, 17232112 and 17232133
Expiration Date(s): Aug-25, Aug-25, May-26, May-26, Sep-26 and Sep-26

What you should do:

• Check your prescription label to see if you have any PRAVASTATIN SODIUM in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 04/16/2025, NORTHSTAR RX LLC recalled PRAVASTATIN SODIUM 20 MG due to CGMP Deviations. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: PRAVASTATIN SODIUM 20 MG
NDC Number: 68462019605
Lot Number(s): 17230810, 17230811, 17230810, 17232501 and 17232502
Expiration Date(s): Mar-26, Mar-26, Mar-26, Nov-26 and Nov-26

What you should do:

• Check your prescription label to see if you have any PRAVASTATIN SODIUM in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 04/16/2025, NORTHSTART RX LLC recalled PRAVASTATIN SODIUM 20 MG due to CGMP Deviations. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: PRAVASTATIN SODIUM 20 MG
NDC Number: 16714055901
Lot Number(s): 17230810
Expiration Date(s): Mar-26

What you should do:

• Check your prescription label to see if you have any PRAVASTATIN SODIUM in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 04/16/2025, GLENMARK PHARMACEUTICALS recalled ROSUVASTATIN CALCIUM 40 MG due to CGMP Deviations. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: ROSUVASTATIN CALCIUM 40 MG
NDC Number: 68462026430
Lot Number(s): 17240389, 17240390, 17240426, 17240427, 17240428, 17240778, 17241055, 17241074, 17241075, 17241091 and 17241100
Expiration Date(s): Feb-26, Feb-26, Feb-26, Feb-26, Feb-26, Apr-26, May-26, Jun-26, Jun-26, Jun-26 and Jun-26

What you should do:

• Check your prescription label to see if you have any ROSUVASTATIN CALCIUM in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 04/16/2025, GLENMARK PHARMACEUTICALS recalled PROPAFENONE HCL ER 225 MG due to CGMP Deviations. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: PROPAFENONE HCL ER 225 MG
NDC Number: 16714082501
Lot Number(s): 17230819
Expiration Date(s): Mar-25

What you should do:

• Check your prescription label to see if you have any PROPAFENONE HCL in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 04/16/2025, GLENMARK PHARMACEUTICALS recalled SAXAGLIPTIN HCL 2.5 MG due to CGMP Deviations. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: SAXAGLIPTIN HCL 2.5 MG
NDC Number: 68462072690
Lot Number(s): 17241788, 17241821 and 17241822
Expiration Date(s): Sep-26, Sep-26 and Sep-26

What you should do:

• Check your prescription label to see if you have any SAXAGLIPTIN HCL in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 04/16/2025, GLENMARK PHARMACEUTICALS recalled SAXAGLIPTIN HCL 2.5 MG due to CGMP Deviations. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: SAXAGLIPTIN HCL 2.5 MG
NDC Number: 68462072630
Lot Number(s): 17241788, 17241821 and 17241822
Expiration Date(s): Sep-26, Sep-26 and Sep-26

What you should do:

• Check your prescription label to see if you have any SAXAGLIPTIN HCL in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 04/16/2025, GLENMARK PHARMACEUTICALS recalled SOLIFENACIN SUCCINATE 10 MG due to CGMP Deviations. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: SOLIFENACIN SUCCINATE 10 MG
NDC Number: 68462038730
Lot Number(s): 17230762
Expiration Date(s): Mar-25

What you should do:

• Check your prescription label to see if you have any SOLIFENACIN SUCCINATE in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 04/16/2025, GLENMARK PHARMACEUTICALS recalled SOLIFENACIN SUCCINATE 10 MG due to CGMP Deviations. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: SOLIFENACIN SUCCINATE 10 MG
NDC Number: 68462038790
Lot Number(s): 17230762
Expiration Date(s): Mar-25

What you should do:

• Check your prescription label to see if you have any SOLIFENACIN SUCCINATE in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 04/16/2025, ZYDUS PHARMACEUTICALS recalled VENLAFAXINE HCL 75 MG due to the Presence of Foreign Substance: Product complaint received for the presence of foreign material embedded resembling a metal shaving in one tablet. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: VENLAFAXINE HCL 75 MG
NDC Number: 68382002101
Lot Number(s): M314265
Expiration Date(s): 10/31/2025

What you should do:

• Check your prescription label to see if you have any VENLAFAXINE HCL in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 04/02/2025, Strides Pharma, INC recalled TESTOSTERONE 25MG(1%) due to the Presence of foreign substance: Presence of Benzene. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: TESTOSTERONE 25MG(1%)
NDC Number: 64380015102
Lot Number(s): 5501127A, 5501236A, 5501341A, 5501406A, 5501408A, 5501516A, 5501568A, 5501829A, 5502000A, 5502004A, 5502005A, 5502092A, 5502217A and 5502262A
Expiration Date(s): Apr-25, Jun-25, Jul-25, Aug-25, Sep-25, Oct-25, Mar-26, Jul-26, Aug-26, Oct-26, Dec-26 and Jan-27

What you should do:

• Check your prescription label to see if you have any TESTOSTERONE in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 04/07/2025, Strides Pharma, INC, recalled TESTOSTERONE 50 MG (1%) due to the Presence of foreign substance: Presence of Benzene. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm. 

Detailed information about the medication is listed below: 

Recalled Drug: TESTOSTERONE50 MG (1%)
NDC Number: 64380015202
Lot Number(s): 5501103A, 5501237A, 5501238A, 5501278A, 5501280A, 5501342A, 5501372A, 5501496A, 5501499A, 5501580A, 5501582A, 5501653A, 5501656A, 5501770A, 5501842A, 5501868A, 5501882A, 5501957A, 5502001A, 5502033A, 5502112A, 5502115A, 5502180A and  5502181A
Expiration Date(s): Mar-25, Apr-25, May-25, Jun-25, Jul-25, Aug-25, Sep-25, Oct-25, Dec-25, Jan-26, Feb-26, Apr-26, May-26, Jul-26, Aug-26, Oct-26 and Nov-26.

What you should do:

• Check your prescription label to see if you have any TESTOSTERONE in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178. 

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 1/15/2025 ENDO USA, INC recalled CLONAZEPAM 0.25 MG due to Labeling: Label Error on Declared Strength; Some cartons were incorrectly labeled. The blister strips inside the product carton reflect the correct strength. The U.S. Food and Drug Administration (FDA) has issued a Class I Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: CLONAZEPAM 0.25 MG ODT TABLET
NDC Number: 49884030702
Lot Number(s): 550142801, 550142901, 550143001, 550143101, 550143201, 550143301, 550143401, 550147201 AND 550147401
Expiration Date(s): 08/31/2026

What you should do:

• Check your prescription label to see if you have any CLONAZEPAM in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 1/15/2025 ENDO USA, INC recalled CLONAZEPAM 1 MG due to Labeling: Label Error on Declared Strength; Some cartons were incorrectly labeled. The blister strips inside the product carton reflect the correct strength. The U.S. Food and Drug Administration (FDA) has issued a Class I Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: CLONAZEPAM 1 MG ODT TABLET
NDC Number: 49884030902
Lot Number(s): 550145201,550175901, 550176001 AND 550176201
Expiration Date(s): 08/31/2026 AND 02/28/2027

What you should do:

• Check your prescription label to see if you have any CLONAZEPAM in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178.

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).

On 01/08/2025 Lupin Pharmaceuticals recalled LEVOTHYROXINE SODIUM 75 MCG due to Failed Impurities/Degradation Specifications: Out of specifications result observed in the drug substance for impurity test during 3-month long term stability study. The U.S. Food and Drug Administration (FDA) has issued a Class II Recall of the affected medications.

More information about the recall is available at: https://www.fda.gov/Safety/Recalls/EnforcementReports/default.htm.

Detailed information about the medication is listed below:

Recalled Drug: LEVOTHYROXINE SODIUM75 MCG
NDC Number: 68180096703
Lot Number(s): LA01276
Expiration Date(s): 07/2026

What you should do:

• Check your prescription label to see if you have any LEVOTHYROXINE SODIUM in the affected lot numbers and expiration dates.
• If you have the medication, contact the pharmacy that you received it from. Any adverse events from the use of prescription drugs should be reported to FDA by visiting www.fda.gov/medwatch/report.htm or calling toll free 1-800-FDA-0178. 

Should you have any questions related to this notice, please contact Customer Service toll free at 1-866-907-1906 (TTY-711).