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
2 this month

Showing 2621–2640 of 17,529 recalls

December 27, 2022· Sentara Infusion Services

Recalled Item: ETHANOL 70% 0.5ML SYRINGE

The Issue: Lack of sterility assurance

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

Class II — Potential Health HazardTerminated
Refund
December 27, 2022· Sentara Infusion Services

Recalled Item: DAPTOMYCIN (a) 400MG IN NS 20ML

The Issue: Lack of sterility assurance

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

Class II — Potential Health HazardTerminated
Refund
December 27, 2022· Sentara Infusion Services

Recalled Item: TPN (a) 115GM/AA

The Issue: Lack of sterility assurance

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

Class II — Potential Health HazardTerminated
Refund
December 27, 2022· Sentara Infusion Services

Recalled Item: AMPICILLIN 12GM IN NS 600M

The Issue: Lack of sterility assurance

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

Class II — Potential Health HazardTerminated
Refund
December 27, 2022· Sentara Infusion Services

Recalled Item: Amikacin 450MG IN NS 45ML

The Issue: Lack of sterility assurance

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

Class II — Potential Health HazardTerminated
Refund
December 27, 2022· Sentara Infusion Services

Recalled Item: INTRALIPID 18GM

The Issue: Lack of sterility assurance

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

Class II — Potential Health HazardTerminated
Refund
December 27, 2022· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Prochlorperazine Maleate Tablets

The Issue: Subpotent Drug: Out of specification for assay at

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

Class III — Low RiskTerminated
Refund
December 23, 2022· GFA Production Xiamen Co. Ltd.

Recalled Item: Adventure Marine 150

The Issue: Microbial Contamination of Non-Sterile Products: FDA Laboratory results

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

Class I — Serious Health HazardTerminated
Refund
December 23, 2022· GFA Production Xiamen Co. Ltd.

Recalled Item: Easy Care First Aid Class A ANSI 25 Person

The Issue: Microbial Contamination of Non-Sterile Products: FDA Laboratory results

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

Class I — Serious Health HazardTerminated
Refund
December 23, 2022· GFA Production Xiamen Co. Ltd.

Recalled Item: Adventure First Aid 1.5

The Issue: Microbial Contamination of Non-Sterile Products: FDA Laboratory results

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

Class I — Serious Health HazardTerminated
Refund
December 23, 2022· GFA Production Xiamen Co. Ltd.

Recalled Item: Easy Care First Aid 25 Person 2009 ANSI

The Issue: Microbial Contamination of Non-Sterile Products: FDA Laboratory results

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

Class I — Serious Health HazardTerminated
Refund
December 23, 2022· GFA Production Xiamen Co. Ltd.

Recalled Item: Easy Care First Aid 10 Person 2009 ANSI

The Issue: Microbial Contamination of Non-Sterile Products: FDA Laboratory results

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

Class I — Serious Health HazardTerminated
Refund
December 23, 2022· GFA Production Xiamen Co. Ltd.

Recalled Item: CVS First Aid Home

The Issue: Microbial Contamination of Non-Sterile Products: FDA Laboratory results

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

Class I — Serious Health HazardTerminated
Refund
December 23, 2022· GFA Production Xiamen Co. Ltd.

Recalled Item: Easy Care First Aid 25 Person 2009 ANSI

The Issue: Microbial Contamination of Non-Sterile Products: FDA Laboratory results

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

Class I — Serious Health HazardTerminated
Refund
December 23, 2022· GFA Production Xiamen Co. Ltd.

Recalled Item: Easy Care First Aid 10 Person 2009 ANSI

The Issue: Microbial Contamination of Non-Sterile Products: FDA Laboratory results

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

Class I — Serious Health HazardTerminated
Refund
December 23, 2022· GFA Production Xiamen Co. Ltd.

Recalled Item: Adventure First Aid 1.0

The Issue: Microbial Contamination of Non-Sterile Products: FDA Laboratory results

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

Class I — Serious Health HazardTerminated
Refund
December 23, 2022· GFA Production Xiamen Co. Ltd.

Recalled Item: Easy Care first aid Burn Cream (benzalkonium chloride 0.13% and

The Issue: Microbial Contamination of Non-Sterile Products: FDA Laboratory results

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

Class I — Serious Health HazardTerminated
Refund
December 22, 2022· Pharmacy Innovations

Recalled Item: Minoxidil 0.75% (1.5ML vial) Injectable

The Issue: Lack of Assurance of Sterility: FDA inspection revealed

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

Class II — Potential Health HazardTerminated
Refund
December 22, 2022· Pharmacy Innovations

Recalled Item: Buprenorphine HCL 0.9 MG/ML (25ML vial) Injectable

The Issue: Lack of Assurance of Sterility: FDA inspection revealed

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

Class II — Potential Health HazardTerminated
Refund
December 22, 2022· Pharmacy Innovations

Recalled Item: Clindamycin/EDTA Calcium 4.1667MG/0.333MG/ML (30ML syringe) Irrigation

The Issue: Lack of Assurance of Sterility: FDA inspection revealed

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

Class II — Potential Health HazardTerminated
Refund