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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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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

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Prescription medicine1,991 Over-the-counter & supplements377 Mobility & home health182

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

1,991 recalls · newest first

Food & drug recall · FDASeptember 3, 2025Serious

Zydus Pharmaceuticals (USA) Inc — Chlorpromazine Hydrochloride Tablets, USP, 50 mg, 100-count bottle, Rx only

Prescription medicine · Zydus Pharmaceuticals (USA) Inc · N/A affected

CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit

Food & drug recall · FDASeptember 2, 2025Serious

AvKARE — Norgestimate and Ethinyl Estradiol Tablets, USP, 0.18 mg/0.025 mg, 0.215 mg/0.025 mg, and 0.25 mg/0.025 mg, 3 Units, 3x28 tablets blister cards per carton, Rx only

Prescription medicine · AvKARE · 2192 cartons affected

Failed Content Uniformity Specifications

Food & drug recall · FDASeptember 2, 2025Serious

The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories — Sulfamethoxazole and Trimethoprim, USP, 800 mg/160 mg, Double Strength, 100 Tablets unit dose blister packs (10x10) per carton, Rx only, Packaged and Distributed

Prescription medicine · The Harvard Drug Group LLC dba Major… · N/A affected

Presence of a Foreign Substance: A specific lot of auxiliary polyester coil, used in product packaging by manufacturer (Amneal Pharmaceuticals LLC)…

Food & drug recall · FDASeptember 2, 2025Serious

The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories — Sulfamethoxazole and Trimethoprim, USP, 800 mg/160 mg, Double Strength, 10 Tablets unit dose blister pack (10x1) per bag, Rx only

Prescription medicine · The Harvard Drug Group LLC dba Major… · N/A affected

Presence of a Foreign Substance: A specific lot of auxiliary polyester coil, used in product packaging by manufacturer (Amneal Pharmaceuticals LLC)…

Food & drug recall · FDAAugust 29, 2025Serious

Fagron Compounding Services — bevacizumab (Avastin) Injection, 1.25mg/0.05mL (0.12 mL Fill), Sterile Single-Dose Syringe, Fagron Sterile Services, 8710 E 34th St N. Wichita, KS 67226

Prescription medicine · Fagron Compounding Services · 109,320 syringes affected

Lack of Assurance of Sterility

Food & drug recall · FDAAugust 28, 2025Labelling issue

Granules Pharmaceuticals Inc. — Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate, Extended-Release Capsules, (Mixed Salts of a Single Entity Amphetamine Product), 5 mg, 100 C

Prescription medicine · Granules Pharmaceuticals Inc. · 3,384 bottles affected

Failed Impurities/Degradation Specifications:

Food & drug recall · FDAAugust 28, 2025Labelling issue

Granules Pharmaceuticals Inc. — Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate, Extended-Release Capsules, (Mixed Salts of a Single Entity Amphetamine Product), 10 mg, 100

Prescription medicine · Granules Pharmaceuticals Inc. · 11,895 bottles affected

Failed Impurities/Degradation Specifications:

Food & drug recall · FDAAugust 28, 2025Serious

Ascend Laboratories, LLC — Aripiprazole Tablets, USP, 10 mg, 30-count bottles, Rx only

Prescription medicine · Ascend Laboratories, LLC · 2,256 bottles affected

Superpotent drug

Food & drug recall · FDAAugust 28, 2025Labelling issue

Granules Pharmaceuticals Inc. — Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate, Extended-Release Capsules, (Mixed Salts of a Single Entity Amphetamine Product), 20 mg, 100

Prescription medicine · Granules Pharmaceuticals Inc. · 11,909 bottles affected

Failed Impurities/Degradation Specifications:

Food & drug recall · FDAAugust 28, 2025Labelling issue

Granules Pharmaceuticals Inc. — Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate, Extended-Release Capsules, (Mixed Salts of a Single Entity Amphetamine Product), 15 mg, 100

Prescription medicine · Granules Pharmaceuticals Inc. · 9,917 bottles affected

Failed Impurities/Degradation Specifications:

Food & drug recall · FDAAugust 28, 2025Labelling issue

Granules Pharmaceuticals Inc. — Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate and Amphetamine Sulfate, Extended-Release Capsules, (Mixed Salts of a Single Entity Amphetamine Product), 30 mg, 100

Prescription medicine · Granules Pharmaceuticals Inc. · 11,928 bottles affected

Failed Impurities/Degradation Specifications:

Food & drug recall · FDAAugust 28, 2025Highest risk

Green Lumber Holdings, LLC — Green Lumber Natural Fuel For Men capsule, packaged in 2, 4, 10, and 30-count blister packs. GreenLumber.com, 2618 San Miguel Drive, Suite #296, Newport Beach, CA 92660

Prescription medicine · Green Lumber Holdings, LLC · N/A affected

Marketed without an Approved NDA/ANDA: FDA analysis found this product to contain tadalafil

Food & drug recall · FDAAugust 27, 2025Serious

Amerisource Health Services LLC — chlorproMAZINE Hydrochloride Tablets, USP, 25 mg, packaged as a) 50 (5x10) blisterpacks, NDC: 60687-430-65; (Individual Dose NDC: 60687-430-11); b) 100 (10x10) blisterpacks, NDC: 60687-430-01, (Individual D

Prescription medicine · Amerisource Health Services LLC · 2,708 cartons affected

Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging at the manufacturing site, was detected with…

Food & drug recall · FDAAugust 27, 2025Serious

Amerisource Health Services LLC — chlorproMAZINE Hydrochloride Tablets, USP, 100 mg, 100 (10x10) blisterpack per carton, Rx Only

Prescription medicine · Amerisource Health Services LLC · 1,757 cartons affected

Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging at the manufacturing site, was detected with…

Food & drug recall · FDAAugust 27, 2025Serious

Amerisource Health Services LLC — chlorproMAZINE Hydrochloride Tablets, USP, 50 mg, 100 (10x10) blisterpacks, Rx Only

Prescription medicine · Amerisource Health Services LLC · 1,062 cartons affected

Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging at the manufacturing site, was detected with…

Food & drug recall · FDAAugust 27, 2025Serious

DermaRite Industries, LLC — McKesson Skin Protectant, Lanolin USP, packaged in a) 5g (NDC 68599-6202-1), and b) 4oz NDC 68599-6203-4 tube

Prescription medicine · DermaRite Industries, LLC · 5,876 units affected

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

Food & drug recall · FDAAugust 27, 2025Serious

Zydus Pharmaceuticals (USA) Inc — Succinylcholine Chloride Injection, USP 200 mg/10 mL (20 mg/mL), Rx only, 10 mL Multiple-dose Vial, Sterile

Prescription medicine · Zydus Pharmaceuticals (USA) Inc · 270,125 Vials affected

Failed Impurities/Degradation Specifications: Out-of-Specification test results obtained for any individual unknown degradation impurity.

Food & drug recall · FDAAugust 27, 2025Serious

DermaRite Industries, LLC — UltraSure Anti-Perspirant & Deodorant, Aluminum Sesquichlorohydrate 15%, 118 mL (4 fl. oz.), DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-266-04

Prescription medicine · DermaRite Industries, LLC · 37,379 spray bottles affected

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

Food & drug recall · FDAAugust 27, 2025Serious

DermaRite Industries, LLC — 4-N-1 Skin Protectant, No Rinse Wash Cream with Dimethicone 1%, 113g, (4 oz) per bottle, DermaRite Industries LLC, 7777 West Side Avenue, North Bergen, NJ 07047. NDC 61924-208-04

Prescription medicine · DermaRite Industries, LLC · 3,178 bottles affected

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

Food & drug recall · FDAAugust 27, 2025Serious

DermaRite Industries, LLC — Lantiseptic, Dry Skin Therapy, Lanolin USP 30%, packaged in a) 5 g (0.17 oz) (NDC 61924-504-05), b) 4 oz (NDC 61924-504-04), and c)14 oz (NDC 61924-710-14) tubes, DermaRite Industries LLC, 7777 West Side Avenue

Prescription medicine · DermaRite Industries, LLC · 8,378 containers affected

CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.

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