Drug Recalls

Here you'll find every drug recall the FDA has issued, including prescription medications, over-the-counter drugs, compounded pharmacy products, and dietary supplements. We've been tracking these since 2006 and our database updates several times a day so you're always looking at current information.

Drugs get recalled for a number of reasons: contamination during manufacturing, incorrect potency or dosage, failed quality testing (like dissolution or stability tests), sterility problems in injectable products, or labeling and packaging errors that could cause someone to take the wrong dose. If you find a product on this list that you use, please follow the instructions provided by the FDA to take the necessary precautions.

17,529 total recalls
1 this month

Showing 6421–6440 of 17,529 recalls

October 1, 2019· Dr. Reddy's Laboratories, Inc.

Recalled Item: Ranitidine Tablets

The Issue: CGMP Deviations: Presence of NDMA impurity detected in

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardCompleted
Refund
October 1, 2019· Dr. Reddy's Laboratories, Inc.

Recalled Item: Dr. Reddy's Ranitidine Capsules

The Issue: CGMP Deviations: Presence of NDMA impurity detected in

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardCompleted
Refund
October 1, 2019· Dr. Reddy's Laboratories, Inc.

Recalled Item: Ranitidine Tablets

The Issue: CGMP Deviations: Presence of NDMA impurity detected in

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardCompleted
Refund
October 1, 2019· Dr. Reddy's Laboratories, Inc.

Recalled Item: Ranitidine Tablets

The Issue: CGMP Deviations: Presence of NDMA impurity detected in

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardCompleted
Refund
September 27, 2019· Arbor Pharmaceuticals Inc.

Recalled Item: Testosterone Cypionate Injection

The Issue: Labeling:Label Mix-up: Shipper Carton labelled Testosterone Cypionate Injection,

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskTerminated
Refund
September 27, 2019· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Ibuprofen Oral Suspension USP

The Issue: Presence of Foreign Substance: Ibuprofen Oral Suspension USP

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund
September 27, 2019· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Children's Ibuprofen Oral Suspension USP

The Issue: Presence of Foreign Substance: Ibuprofen Oral Suspension USP

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund
September 27, 2019· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Ibuprofen Oral Suspension USP

The Issue: Presence of Foreign Substance: Ibuprofen Oral Suspension USP

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund
September 27, 2019· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Children's Ibuprofen Oral Suspension USP

The Issue: Presence of Foreign Substance: Ibuprofen Oral Suspension USP

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund
September 27, 2019· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Children's Ibuprofen Oral Suspension USP

The Issue: Presence of Foreign Substance: Ibuprofen Oral Suspension USP

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund
September 26, 2019· Epic Pharma, LLC

Recalled Item: Estradiol tablets

The Issue: Presence of Foreign Tablets/Capsules: Estradiol 1 mg was

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund
September 26, 2019· Alkermes, Inc.

Recalled Item: Vivitrol (naltrexone for extended-release injectable suspension) 380...

The Issue: Labeling: Not Elsewhere Classified. Drug product kit recalled

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardTerminated
Refund
September 24, 2019· Apotex Inc.

Recalled Item: Equate Maximum Strength Ranitidine Tablets

The Issue: GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine (ND

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardCompleted
Refund
September 24, 2019· Apotex Inc.

Recalled Item: Equate Maximum Strength Ranitidine Tablets

The Issue: GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine (ND

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardCompleted
Refund
September 24, 2019· Apotex Inc.

Recalled Item: Rite Aid Pharmacy Maximum Strength Ranitidine Tablets

The Issue: GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine (ND

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardCompleted
Refund
September 24, 2019· Apotex Inc.

Recalled Item: Rite Aid Pharmacy Maximum Strength Ranitidine Tablets

The Issue: GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine (ND

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardCompleted
Refund
September 24, 2019· Apotex Inc.

Recalled Item: Walgreens Regular Strength Wal-Zan 75 Ranitidine Tablets

The Issue: GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine (ND

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardCompleted
Refund
September 24, 2019· Apotex Inc.

Recalled Item: Walgreens Maximum Strength Wal-Zan 150 Ranitidine Tablets

The Issue: GGMP Deviations: Possible contamination with impurity N-nitrosodimethylamine (ND

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardCompleted
Refund
September 24, 2019· Amneal Pharmaceuticals, Inc.

Recalled Item: Benazepril HCl Tablets

The Issue: Presence of Foreign Tablet/Capsule; Promethazine HCl tablet found

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskTerminated
Refund
September 23, 2019· AuroMedics Pharma LLC

Recalled Item: Ranitidine Tablets USP

The Issue: CGMP DEVIATIONS: One lot of Ranitidine Tablets USP,

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund