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 16801–16820 of 17,529 recalls

March 18, 2013· Physicians Total Care, Inc.

Recalled Item: Camila 0.35 mg Tablets

The Issue: Failed Impurity/Degradation Specification; an impurity identified as N-Butyl-Ben

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

Class III — Low RiskTerminated
Refund
March 18, 2013· West-ward Pharmaceutical Corp.

Recalled Item: Donnatal Extentabs

The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date:

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

Class II — Potential Health HazardTerminated
Refund
March 18, 2013· Reckitt Benckiser Inc

Recalled Item: Cherry Cepacol Sore Throat Lozenges

The Issue: Subpotent Drug: Product did not conform to the

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

Class III — Low RiskTerminated
Refund
March 16, 2013· Tarmac Products, Inc. d.b.a. Axara Pharmaceuticals

Recalled Item: "Well at Wallgreens" Regular Strength Antacid Liquid...

The Issue: E. coli Contamination

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

Class II — Potential Health HazardTerminated
Refund
March 15, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Junel(TM) Fe 1.5/30 (norethindrone acetate and ethinyl estradiol tablets

The Issue: Failed Impurity/Degradation Specification; an impurity identified as N-Butyl-Ben

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

Class III — Low RiskTerminated
Refund
March 15, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Jolessa(R) (levonorgestrel/ethinyl estradiol tablets

The Issue: Failed Impurity/Degradation Specification; an impurity identified as N-Butyl-Ben

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

Class III — Low RiskTerminated
Refund
March 15, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Balziva(TM) (norethindrone and ethinyl estradiol tablets

The Issue: Failed Impurity/Degradation Specification; an impurity identified as N-Butyl-Ben

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

Class III — Low RiskTerminated
Refund
March 15, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Lessina(R) (Levonorgestrel and ethinyl estradiol tablets

The Issue: Failed Impurity/Degradation Specification; an impurity identified as N-Butyl-Ben

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

Class III — Low RiskTerminated
Refund
March 15, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Camila (norethindrone tablets

The Issue: Failed Impurity/Degradation Specification; an impurity identified as N-Butyl-Ben

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

Class III — Low RiskTerminated
Refund
March 15, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Errin (norethindrone tablets

The Issue: Failed Impurity/Degradation Specification; an impurity identified as N-Butyl-Ben

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

Class III — Low RiskTerminated
Refund
March 14, 2013· Med Prep Consulting, Inc.

Recalled Item: Magnesium Sulfate 2 grams in Dextrose 5% for Injection

The Issue: Non-Sterility; mold contamination

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

Class I — Serious Health HazardTerminated
Refund
March 14, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Camrese(TM) (Levonorgestrel/Ethinyl Estradiol Tablets)

The Issue: Failed Impurity/Degradation Specifications; an impurity identified as N-Butyl-Be

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

Class III — Low RiskTerminated
Refund
March 14, 2013· Med Prep Consulting, Inc.

Recalled Item: All Compounded Products

The Issue: Lack of Assurance of Sterility; potential for mold

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

Class II — Potential Health HazardTerminated
Refund
March 14, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Seasonale(R) (Levonorgestrel/Ethinyl Estradiol Tablets)

The Issue: Failed Impurity/Degradation Specification; an impurity identified as N-Butyl-Ben

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

Class III — Low RiskTerminated
Refund
March 12, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Jolessa (levonorgestrel/ethinyl estradiol) Tablets

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
March 12, 2013· L. Perrigo Co.

Recalled Item: Liothyronine Sodium Tablets

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
March 12, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Portia (levonorgestrel and ethinyl estradiol) Tablets

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
March 11, 2013· Palmer Natural Products

Recalled Item: Brain Defogger

The Issue: Marketed Without an Approved NDA/ANDA: The products are

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

Class II — Potential Health HazardTerminated
Refund
March 11, 2013· Palmer Natural Products

Recalled Item: Oxiracetam & Choline

The Issue: Marketed Without an Approved NDA/ANDA: The products are

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

Class II — Potential Health HazardTerminated
Refund
March 11, 2013· Palmer Natural Products

Recalled Item: Aniracetam & Choline capsules

The Issue: Marketed Without an Approved NDA/ANDA: The products are

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

Class II — Potential Health HazardTerminated
Refund