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 7401–7420 of 17,529 recalls

April 26, 2019· Advanced Pharma Inc.

Recalled Item: HYDROmorphone 20 mg/100 mL Injectable Solution

The Issue: Sub-potency

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

Class II — Potential Health HazardTerminated
Refund
April 25, 2019· Zydus Pharmaceuticals USA Inc

Recalled Item: Acyclovir Tablets

The Issue: Labeling; Label Mix-up; report received of one bottle

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

Class II — Potential Health HazardTerminated
Refund
April 25, 2019· Zydus Pharmaceuticals USA Inc

Recalled Item: Carvedilol Tablets

The Issue: Labeling; Label Mix-up; report received of one bottle

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

Class II — Potential Health HazardTerminated
Refund
April 25, 2019· Advantice Health

Recalled Item: Dermoplast Anesthetic PAIN & ITCH (benzocaine and menthol) SPRAY canisters

The Issue: Labeling: Not Elsewhere Classified: canisters incorrectly state the

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

Class III — Low RiskTerminated
Refund
April 25, 2019· Advantice Health

Recalled Item: Dermoplast Anesthetic PAIN & ITCH (benzocaine and menthol) SPRAY canisters

The Issue: Labeling: Not Elsewhere Classified: Full cases may contain

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

Class III — Low RiskTerminated
Refund
April 25, 2019· US Worldmeds LLC

Recalled Item: Revonto (dantrolene sodium for injection)

The Issue: Presence of Precipitate: Appearance is Out of Specification

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

Class II — Potential Health HazardTerminated
Refund
April 24, 2019· MAJOR PHARMACEUTICALS

Recalled Item: DIVALPROEX SODIUM EXTENDED-RELEASE TABLETS

The Issue: cGMP deviations: Product was exposed above 50% relative

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

Class II — Potential Health HazardTerminated
Refund
April 24, 2019· AVKARE Inc.

Recalled Item: Losartan Potassium Tablets USP 50 mg 50 tablets (5x10) Unit

The Issue: CGMP Deviations: FDA lab confirmed presence of an

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

Class II — Potential Health HazardOngoing
Refund
April 24, 2019· AVKARE Inc.

Recalled Item: Losartan Potassium Tablets USP 25 mg 50 tablets (5x10) Unit

The Issue: CGMP Deviations: FDA lab confirmed presence of an

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

Class II — Potential Health HazardOngoing
Refund
April 24, 2019· Legacy Pharmaceutical Packaging LLC

Recalled Item: Losartan Potassium Tablets

The Issue: CGMP Deviations: Detection of trace amounts of N-Methylnitrosobutyric

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

Class II — Potential Health HazardOngoing
Refund
April 23, 2019· D.B.P. Distribution

Recalled Item: Titanium 4000

The Issue: Undeclared Sildenafil

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

Class I — Serious Health HazardTerminated
Refund
April 23, 2019· Akorn Inc

Recalled Item: Fentanyl Citrate Injection

The Issue: Failed impurities/degradation specification: Out of Specification result for

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

Class III — Low RiskTerminated
Refund
April 22, 2019· Inopak Ltd

Recalled Item: Mild Health Care Antibacterial Hand Soap

The Issue: CGMP Deviations: hand sanitizers and soaps were not

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

Class II — Potential Health HazardTerminated
Refund
April 22, 2019· Inopak Ltd

Recalled Item: Unison Hand Care Products

The Issue: CGMP Deviations: hand sanitizers and soaps were not

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

Class II — Potential Health HazardTerminated
Refund
April 22, 2019· Inopak Ltd

Recalled Item: Antibacterial Hand Soap

The Issue: CGMP Deviations: hand sanitizers and soaps were not

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

Class II — Potential Health HazardTerminated
Refund
April 22, 2019· Inopak Ltd

Recalled Item: INOFOAM Foaming E-2 Food Handling Wash with .6% PCMX

The Issue: CGMP Deviations: hand sanitizers and soaps were not

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

Class II — Potential Health HazardTerminated
Refund
April 22, 2019· Inopak Ltd

Recalled Item: INODERM Antiseptic Hand Soap (E-2)

The Issue: CGMP Deviations: hand sanitizers and soaps were not

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

Class II — Potential Health HazardTerminated
Refund
April 22, 2019· Inopak Ltd

Recalled Item: Antibacterial Hand Soap

The Issue: CGMP Deviations: hand sanitizers and soaps were not

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

Class II — Potential Health HazardTerminated
Refund
April 22, 2019· Inopak Ltd

Recalled Item: Instant Waterless Hand Sanitizer

The Issue: CGMP Deviations: hand sanitizers and soaps were not

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

Class II — Potential Health HazardTerminated
Refund
April 22, 2019· Inopak Ltd

Recalled Item: Sani-Guard-SF Waterless Foam Hand Sanitizer

The Issue: CGMP Deviations: hand sanitizers and soaps were not

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

Class II — Potential Health HazardTerminated
Refund