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The Recall Registry is not a government service and does not issue recalls. We gather published recall notices from the U.S. Consumer Product Safety Commission, the U.S. Food and Drug Administration and the National Highway Traffic Safety Administration, and rewrite them in plain language. Always confirm the details with the issuing agency using the link on each recall page.

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Home › All recalls › Prescription medicine

Prescription medicine recalls

Prescription drugs recalled for contamination, potency or labelling.

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Sleep & nursery274 Car seats254 Formula & baby food230 Children's medicine176 Swings & bouncers125 Nursery furniture317 Toys & play852 Strollers & carriers156 Clothing & sleepwear626

Adults & seniors

Prescription medicine1,993 Over-the-counter & supplements378 Mobility & home health182

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Highest riskSeriousWorth checkingLabelling issueTap any recall for the hazard and what to do

1,993 recalls · newest first

Food & drug recall · FDADecember 17, 2024Serious

Amerisource Health Services LLC — glipiZIDE, Extended-Release Tablets, 2.5 mg, 30-count (3x10 blister cards) carton, Rx Only

Prescription medicine · Amerisource Health Services LLC · 2,028 units (cartons of 30 individual unit doses) affected

Failed Dissolution Specifications:

Food & drug recall · FDADecember 16, 2024Labelling issue

SOMERSET THERAPEUTICS LLC — Atropine Sulfate Ophthalmic Solution, USP 1%, 5 mL bottles, Rx only

Prescription medicine · SOMERSET THERAPEUTICS LLC · 5,870 bottles affected

Failed Impurities/Degradation Specifications

Food & drug recall · FDADecember 16, 2024Serious

FDC Limited — Ciprofloxacin Ophthalmic Solution USP, 0.3% as base, Sterile, package in 5 mL bottles, Rx Only

Prescription medicine · FDC Limited · 136,181 bottles affected

Defective container: Unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle

Food & drug recall · FDADecember 13, 2024Serious

Amerisource Health Services LLC — Clobazam Tablets, 10 mg, packaged in 30 tablets per carton (3x10 blister cards each), Rx Only, Amneal Pharmaceuticals LLC

Prescription medicine · Amerisource Health Services LLC · 5,178 cartons affected

Presence of Foreign Tablets/Capsules

Food & drug recall · FDADecember 12, 2024Serious

Ascend Laboratories, LLC — Dabigatran Etexilate, 150mg capsules, 60-count bottles, Rx Only

Prescription medicine · Ascend Laboratories, LLC · 10,444 bottles affected

CGMP Deviations: Presence of N-nitroso-Dabigatran impurity above recommended interim limit

Food & drug recall · FDADecember 12, 2024Highest risk

GNMart LLC — FORCE FOREVER 400mg Tablets, Huesos y articulaciones sin dolor, SUPLEMENTO ALIMENTICIO, 60-count bottles

Prescription medicine · GNMart LLC · 374 bottles affected

Marketed without an approved NDA/ANDA.

Food & drug recall · FDADecember 12, 2024Labelling issue

Akron Pharma, Inc. — Diphenhydramine HCl 25 mg, 1000 Capsules per bottle, Akron Pharma

Prescription medicine · Akron Pharma, Inc. · 456 bottles affected

Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.

Food & drug recall · FDADecember 12, 2024Serious

Ascend Laboratories, LLC — Dabigatran Etexilate, 75 mg capsules, 60-count bottles, Rx Only

Prescription medicine · Ascend Laboratories, LLC · 1971 bottles affected

CGMP Deviations: Presence of N-nitroso-Dabigatran impurity above recommended interim limit

Food & drug recall · FDADecember 12, 2024Labelling issue

Akron Pharma, Inc. — Diphenhydramine HCl 25 mg, 100 capsules per bottle, Akron Pharma

Prescription medicine · Akron Pharma, Inc. · 7198 bottles affected

Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.

Food & drug recall · FDADecember 12, 2024Labelling issue

Akron Pharma, Inc. — Diphenhydramine HCl 50 mg, 1000 capsules per bottle, Akron Pharma

Prescription medicine · Akron Pharma, Inc. · 324 bottles affected

Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.

Food & drug recall · FDADecember 11, 2024Serious

Glenmark Pharmaceuticals Inc., USA — chlorproMAZINE Hydrochloride Tablets, USP, 25 mg, 100-count bottle, RX only

Prescription medicine · Glenmark Pharmaceuticals Inc., USA

CGMP Deviations: N-Nitroso-Desmethyl Chlorpromazine impurity (NNDCI) were found to be failing per current FDA recommended limit.

Food & drug recall · FDADecember 11, 2024Serious

Glenmark Pharmaceuticals Inc., USA — chlorproMAZINE Hydrochloride Tablets, USP, 10mg, 100-count bottle, RX only

Prescription medicine · Glenmark Pharmaceuticals Inc., USA · 3,888 affected

CGMP Deviations: N-Nitroso-Desmethyl Chlorpromazine impurity (NNDCI) were found to be failing per current FDA recommended limit.

Food & drug recall · FDADecember 10, 2024Serious

Regenerative Processing Plant, LLC — LITE Regener-Eyes, Ophthalmic Solution (glycerin 0.4%), 3mL bottles

Prescription medicine · Regenerative Processing Plant, LLC · 170812 bottles affected

Lack of Sterility Assurance

Food & drug recall · FDADecember 10, 2024Serious

Regenerative Processing Plant, LLC — PROFESSIONAL Regener-Eyes, Ophthalmic Solution (glycerin 0.5%) , 3mL bottles

Prescription medicine · Regenerative Processing Plant, LLC · 59275 affected

Lack of Sterility Assurance

Food & drug recall · FDADecember 10, 2024Serious

VIONA PHARMACEUTICALS INC — Dapsone Gel 7.5%, 90 g, Rx Only

Prescription medicine · VIONA PHARMACEUTICALS INC · 2760 packs affected

Crystallization

Food & drug recall · FDADecember 10, 2024Serious

VIONA PHARMACEUTICALS INC — Dapsone Gel 7.5%, 60 g, Rx Only

Prescription medicine · VIONA PHARMACEUTICALS INC · 23304 packs affected

Crystallization

Food & drug recall · FDADecember 6, 2024Serious

Breckenridge Pharmaceutical, Inc — Duloxetine Delayed-Release Capsules, USP, 30mg, Rx Only, 90-count bottles (NDC 51991-747-90) Mfr. by: Towa Pharmaceutical Europe, S.L. Martorelles, (Barcelona), Spain, Dist. by: Breckenridge Pharmaceutical

Prescription medicine · Breckenridge Pharmaceutical, Inc · 163,883 bottles affected

CGMP Deviations: presence of N-nitroso-duloxetine impurity above FDA recommended interim limit.

Food & drug recall · FDADecember 6, 2024Serious

Breckenridge Pharmaceutical, Inc — Duloxetine Delayed-Release Capsules, USP, 60 mg, Rx Only, 90-count bottles (NDC 51991-748-90) Mfr. by: Towa Pharmaceutical Europe, S.L. Martorelles, (Barcelona), Spain, Dist. by: Breckenridge Pharmaceutica

Prescription medicine · Breckenridge Pharmaceutical, Inc · 76,968 bottles affected

CGMP Deviations: presence of N-nitroso-duloxetine impurity above FDA recommended interim limit.

Food & drug recall · FDADecember 6, 2024Serious

Amerisource Health Services LLC — Duloxetine Delayed-Release Capsules USP, 60 mg, Rx only, 30 count bottles

Prescription medicine · Amerisource Health Services LLC · 20,734 30-count bottles affected

CGMP Deviations: Presence of N-nitroso-duloxetine impurity above the recommended interim limit.

Food & drug recall · FDADecember 6, 2024Serious

Amerisource Health Services LLC — Duloxetine Delayed-Release Capsules USP, 30 mg, Rx only, 30 count bottles

Prescription medicine · Amerisource Health Services LLC · 21,262 bottles affected

CGMP Deviations: Presence of N-nitroso-duloxetine impurity above the recommended interim limit.

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