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
0 this month

Showing 9421–9440 of 17,529 recalls

February 5, 2018· PharMEDium Services, LLC

Recalled Item: 15 units Oxytocin added to 0.9% Sodium Chloride Injection

The Issue: Lack of assurance of sterility: Three lots were

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

Class II — Potential Health HazardTerminated
Refund
February 2, 2018· Aurobindo Pharma Ltd.

Recalled Item: Metformin Hydrochloride Tablets

The Issue: Presence of Foreign Tablet: Metformin BP 1000mg was

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

Class III — Low RiskTerminated
Refund
February 2, 2018· ALLERGAN

Recalled Item: NORCO (Hydrocodone Bitartrate and Acetaminophen) Tablets

The Issue: Labeling: Not Elsewhere Classified: does not have the

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

Class III — Low RiskTerminated
Refund
January 30, 2018· Millennium Pharmaceuticals Inc.

Recalled Item: VELCADE (bortezomib) for injection

The Issue: Defective Container: Confirmed reports of loose vial crimps

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

Class II — Potential Health HazardTerminated
Refund
January 29, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium Tablets 40 mg

The Issue: Failed Impurities/Degradations Specifications; out-of-specification results obse

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

Class III — Low RiskTerminated
Refund
January 29, 2018· Teva Pharmaceuticals USA

Recalled Item: Fentanyl Transdermal System. 25 mcg/h

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
January 29, 2018· Teva Pharmaceuticals USA

Recalled Item: Fentanyl Transdermal System

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
January 29, 2018· Teva Pharmaceuticals USA

Recalled Item: Fentanyl Transdermal System

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
January 29, 2018· Mckesson Packaging Services

Recalled Item: Megestrol Acetate Oral Suspension

The Issue: Subpotent Drug: Out of specification for assay (stability

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

Class III — Low RiskTerminated
Refund
January 29, 2018· Teva Pharmaceuticals USA

Recalled Item: Fentanyl Transdermal System. 75 mcg/h

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
January 29, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium Tablets 10 mg

The Issue: Failed Impurities/Degradations Specifications; out-of-specification results obse

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

Class III — Low RiskTerminated
Refund
January 29, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Atorvastatin Calcium Tablets 20 mg

The Issue: Failed Impurities/Degradations Specifications; out-of-specification results obse

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

Class III — Low RiskTerminated
Refund
January 26, 2018· Primus Pharmaceuticals, Inc.

Recalled Item: Limbrel (flavocoxid 500 mg) capsules

The Issue: Marketed Without An Approved NDA/ANDA: Based on the

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

Class I — Serious Health HazardTerminated
Refund
January 26, 2018· Primus Pharmaceuticals, Inc.

Recalled Item: Limbrel (flavocoxid 250 mg) capsules

The Issue: Marketed Without An Approved NDA/ANDA: Based on the

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

Class I — Serious Health HazardTerminated
Refund
January 26, 2018· Primus Pharmaceuticals, Inc.

Recalled Item: Limbrel250 (flavocoxid and citrated zinc bisglycinate) 250 mg/50 mg capsules

The Issue: Marketed Without An Approved NDA/ANDA: Based on the

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

Class I — Serious Health HazardTerminated
Refund
January 26, 2018· Primus Pharmaceuticals, Inc.

Recalled Item: Limbrel500 (flavocoxid and citrated zinc bisglycinate) 500 mg/50 mg capsules

The Issue: Marketed Without An Approved NDA/ANDA: Based on the

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

Class I — Serious Health HazardTerminated
Refund
January 25, 2018· PD-Rx Pharmaceuticals, Inc.

Recalled Item: PD-Rx Pharmaceuticals Incorporated Ibuprofen 200 mg tablets a) 24 tablets

The Issue: CGMP deviations

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

Class II — Potential Health HazardTerminated
Refund
January 24, 2018· Oxygen Development Llc

Recalled Item: Life Brand Clear Action Acne Treatment Concealer Stick (Salicylic acid)

The Issue: Superpotent drug: failed assay throughout the stick after

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

Class III — Low RiskTerminated
Refund
January 24, 2018· JCB Laboratories LLC

Recalled Item: Cefuroxime

The Issue: Subpotent Drug: The product is sub-potent prior to

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

Class III — Low RiskTerminated
Refund
January 22, 2018· AbbVie Inc.

Recalled Item: Ultane (sevoflurane)

The Issue: Defective container: presence of a hole in the

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

Class III — Low RiskTerminated
Refund