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 2941–2960 of 17,529 recalls

July 15, 2022· Vi-Jon, LLC

Recalled Item: CVS Health

The Issue: Microbial contamination of non-sterile products

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

Class I — Serious Health HazardTerminated
Refund
July 15, 2022· Vi-Jon, LLC

Recalled Item: Magnesium Citrate SALINE LAXATIVE

The Issue: CGMP Deviations

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

Class II — Potential Health HazardTerminated
Refund
July 15, 2022· Vi-Jon, LLC

Recalled Item: Walgreens

The Issue: Microbial contamination of non-sterile products

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

Class I — Serious Health HazardTerminated
Refund
July 15, 2022· Vi-Jon, LLC

Recalled Item: Topcare health

The Issue: Microbial contamination of non-sterile products

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

Class I — Serious Health HazardTerminated
Refund
July 15, 2022· Vi-Jon, LLC

Recalled Item: EQUALINE magnesium citrate saline laxative

The Issue: Microbial contamination of non-sterile products

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

Class I — Serious Health HazardTerminated
Refund
July 15, 2022· Vi-Jon, LLC

Recalled Item: equate Magnesium Citrate

The Issue: Microbial contamination of non-sterile products

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

Class I — Serious Health HazardTerminated
Refund
July 15, 2022· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Fulvestrant Injection 250mg/5mL (50 mg/mL)

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
July 15, 2022· Aire-Master of America Inc

Recalled Item: Common Sense Fragrance Free Hand Sanitizer

The Issue: CGMP Deviations: product manufactured using deionized water from

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

Class II — Potential Health HazardTerminated
Refund
July 15, 2022· Aire-Master of America Inc

Recalled Item: Protect U Guard Foaming Hand Sanitizer Ophardt

The Issue: CGMP Deviations: product manufactured using deionized water from

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

Class II — Potential Health HazardTerminated
Refund
July 15, 2022· Aire-Master of America Inc

Recalled Item: Protect U Guard Foaming Hand Sanitizer

The Issue: CGMP Deviations: product manufactured using deionized water from

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

Class II — Potential Health HazardTerminated
Refund
July 15, 2022· Aire-Master of America Inc

Recalled Item: Avant Foaming Hand Sanitizer Ophardt

The Issue: CGMP Deviations: product manufactured using deionized water from

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

Class II — Potential Health HazardTerminated
Refund
July 15, 2022· Aire-Master of America Inc

Recalled Item: Avant Foaming Hand Sanitizer

The Issue: CGMP Deviations: product manufactured using deionized water from

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

Class II — Potential Health HazardTerminated
Refund
July 15, 2022· Aire-Master of America Inc

Recalled Item: Stage 2-Ophardt Foaming Hand Sanitizer

The Issue: CGMP Deviations: product manufactured using deionized water from

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

Class II — Potential Health HazardTerminated
Refund
July 14, 2022· CIPLA

Recalled Item: Difluprednate Ophthalmic Emulsion

The Issue: Lack of Assurance of Sterility: customer complaint for

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

Class II — Potential Health HazardTerminated
Refund
July 13, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Lansoprazole Delayed-Release Orally Disintegrating Tablets

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
July 13, 2022· Dr. Reddy's Laboratories, Inc.

Recalled Item: Lansoprazole Delayed-Release Orally Disintegrating Tablets

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
July 13, 2022· Pfizer Inc.

Recalled Item: Propofol Injectable Emulsion

The Issue: Presence of particulate matter: particulate identified as a

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

Class I — Serious Health HazardTerminated
Refund
July 11, 2022· Tolmar, Inc.

Recalled Item: Naftifine Hydrochloride Gel

The Issue: Failed Impurities/ degradation specifications: Out-of-Specification test results

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

Class II — Potential Health HazardTerminated
Refund
July 11, 2022· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Tacrolimus Ointment

The Issue: Defective Container: Tube split from side seam

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

Class III — Low RiskOngoing
Refund
July 11, 2022· Hikma Pharmaceuticals USA Inc.

Recalled Item: Ativan Injection (lorazepam injection

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund