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 1561–1580 of 17,529 recalls

October 23, 2023· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Esomeprazole Magnesium Delayed-Release Capsules

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
October 23, 2023· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Ranolazine Extended-Release Tablets 500mg

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardOngoing
Refund
October 20, 2023· Botanical Be

Recalled Item: Artri King con Origa y Omega 3 tablets

The Issue: Undeclared Diclofenac

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

Class I — Serious Health HazardOngoing
Refund
October 20, 2023· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Bisoprolol Fumarate and Hydrochlorothiazide Tablets

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
October 20, 2023· Botanical Be

Recalled Item: Reumo Flex caplets

The Issue: Undeclared Diclofenac

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

Class I — Serious Health HazardOngoing
Refund
October 20, 2023· Omega & Delta Co., Inc.

Recalled Item: DOP Instant Hand Sanitizer (Ethyl Alcohol 65%) with Moisturizers

The Issue: Sub Potent and Super Potent Product: During an

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

Class II — Potential Health HazardOngoing
Refund
October 20, 2023· Botanical Be

Recalled Item: Kuka Flex Forte caplets

The Issue: Undeclared Diclofenac

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

Class I — Serious Health HazardOngoing
Refund
October 20, 2023· ITF PHARMA INC

Recalled Item: Tiglutik (riluzole) Oral Suspension 50 mg/10 mL (5 mg/mL)

The Issue: Failed Viscosity Specifications: Out-of-specification test results for viscosity

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

Class II — Potential Health HazardTerminated
Refund
October 20, 2023· Omega & Delta Co., Inc.

Recalled Item: DOP Instant Hand Sanitizer (Ethyl Alcohol 65%) with Moisturizers

The Issue: Sub Potent and Super Potent Product: During an

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

Class II — Potential Health HazardOngoing
Refund
October 20, 2023· Omega & Delta Co., Inc.

Recalled Item: Equate Hand Sanitizer (Ethyl Alcohol 62%)

The Issue: Sub Potent and Super Potent Product: During an

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

Class II — Potential Health HazardOngoing
Refund
October 20, 2023· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Deferasirox Tablets for Oral Suspension

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardOngoing
Refund
October 20, 2023· Zyla Life Sciences US Inc.

Recalled Item: Oxaydo (oxycodone HCl

The Issue: Sub-potent Drug: Lower potency than labeled

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

Class III — Low RiskOngoing
Refund
October 20, 2023· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Liothyronine Sodium Tablets

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
October 20, 2023· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Liothyronine Sodium Tablets

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
October 20, 2023· Edenbridge Pharmaceuticals, LLC

Recalled Item: Opium Tincture

The Issue: Subpotent Drug

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

Class III — Low RiskTerminated
Refund
October 19, 2023· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Oxybutynin Chloride Extended-Release Tablet USP

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardCompleted
Refund
October 19, 2023· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Oxybutynin Chloride Extended-Release Tablet USP

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardCompleted
Refund
October 19, 2023· Zydus Pharmaceuticals (USA) Inc

Recalled Item: Oxybutynin Chloride Extended-Release Tablet USP

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardCompleted
Refund
October 19, 2023· Safecor Health, LLC

Recalled Item: Strong Iodine Solution U.S.P. (Lugol's Solution) (Iodine 5%)

The Issue: CGMP Deviations: Recall due to the absence of

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

Class II — Potential Health HazardTerminated
Refund
October 18, 2023· Exela Pharma Sciences LLC

Recalled Item: ELCYS (cysteine hydrochloride injection)

The Issue: Presence of Particulate Matter: Silicone

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

Class I — Serious Health HazardOngoing
Refund