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 7961–7980 of 17,529 recalls

November 9, 2018· Ecolab Inc

Recalled Item: Equi-Soft Foam

The Issue: Labeling: Label mix-up - the label on the

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

Class II — Potential Health HazardTerminated
Refund
November 9, 2018· Ecolab Inc

Recalled Item: Medi-Stat Foam

The Issue: Labeling: Label mix-up - the label on the

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

Class II — Potential Health HazardTerminated
Refund
November 9, 2018· AMERICAN HEALTH PACKAGING

Recalled Item: Nitrofurantoin Capsules USP (Monohydrate/Macrocrystals)

The Issue: Cross contamination with other products: This sub-recall is

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

Class III — Low RiskTerminated
Refund
November 8, 2018· ALLERGAN

Recalled Item: INFed (Iron Dextran Injection USP) 100 mg elemental iron/2 mL (50 mg/mL)

The Issue: Failed Stability Specification: out of specification for iron

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

Class II — Potential Health HazardTerminated
Refund
November 8, 2018· Eli Lilly & Co

Recalled Item: ERBITUX CETUXIMAB Injection

The Issue: Labeling: Missing label; potential for missing primary container

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

Class III — Low RiskTerminated
Refund
November 7, 2018· RemedyRepack Inc.

Recalled Item: Nitrofurantoin Monohydrate/Macrocrystals capsules

The Issue: Cross contamination with other products: Product is being

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

Class III — Low RiskTerminated
Refund
November 7, 2018· Dr. Reddy's Laboratories, Inc.

Recalled Item: Clopidogrel Tablets

The Issue: Failed Dissolution Specification: Out-of-Specification results were observed for

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

Class II — Potential Health HazardTerminated
Refund
November 6, 2018· L. Perrigo Company

Recalled Item: Antacid Tablets

The Issue: Presence of foreign substance: Product found to contain

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

Class II — Potential Health HazardTerminated
Refund
November 6, 2018· Takeda Development Center Americas, Inc.

Recalled Item: AMITIZA (lubiprostone) capsules 8 mcg. 60-count bottle

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
November 6, 2018· Breckenridge Pharmaceutical, Inc.

Recalled Item: Megestrol Acetate Oral Suspension

The Issue: Failed Stability Specifications: Out-of-Specification results obtained for parti

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

Class III — Low RiskTerminated
Refund
November 5, 2018· Kadesh International

Recalled Item: puriton EYE RELIEF DROPS

The Issue: Non-Sterility: Product manufactured under non-sterile production conditions

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

Class I — Serious Health HazardTerminated
Refund
November 2, 2018· Bound Tree Medical, LLC

Recalled Item: Curaplex Epi Kit NOT FOR IV USE

The Issue: Labeling Incorrect Instructions: This recall has been initiated

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

Class II — Potential Health HazardTerminated
Refund
November 2, 2018· Bound Tree Medical, LLC

Recalled Item: Curaplex Epi Safe Kit

The Issue: Labeling Incorrect Instructions: This recall has been initiated

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

Class II — Potential Health HazardTerminated
Refund
November 2, 2018· Bound Tree Medical, LLC

Recalled Item: curaplex Epi Safe Administration and Training Kits

The Issue: Labeling Incorrect Instructions: This recall has been initiated

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

Class II — Potential Health HazardTerminated
Refund
November 2, 2018· Bound Tree Medical, LLC

Recalled Item: curaplex Epi Safe Kit

The Issue: Labeling Incorrect Instructions: This recall has been initiated

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

Class II — Potential Health HazardTerminated
Refund
November 2, 2018· Golden State Medical Supply Inc.

Recalled Item: IRBESARTAN Tablets

The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of

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

Class II — Potential Health HazardTerminated
Refund
November 2, 2018· Golden State Medical Supply Inc.

Recalled Item: IRBESARTAN Tablets

The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of

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

Class II — Potential Health HazardTerminated
Refund
November 2, 2018· Golden State Medical Supply Inc.

Recalled Item: IRBESARTAN Tablets

The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of

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

Class II — Potential Health HazardTerminated
Refund
November 2, 2018· Sandoz Inc

Recalled Item: Nitrofurantoin Capsules

The Issue: Cross Contamination with Other Products

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

Class III — Low RiskTerminated
Refund
November 2, 2018· Sandoz Inc

Recalled Item: Nitrofurantoin Capsules

The Issue: Cross Contamination with Other Products

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

Class III — Low RiskTerminated
Refund