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 14161–14180 of 17,529 recalls

November 7, 2014· Perry Drug Inc.

Recalled Item: Testosterone CYP-250/PROP-20 mg

The Issue: Lack of sterility assurance;All lots of sterile products

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

Class II — Potential Health HazardTerminated
Refund
November 7, 2014· Perry Drug Inc.

Recalled Item: HCG - 10

The Issue: Lack of sterility assurance;All lots of sterile products

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

Class II — Potential Health HazardTerminated
Refund
November 7, 2014· Perry Drug Inc.

Recalled Item: 2Ml HCG 10

The Issue: Lack of sterility assurance;All lots of sterile products

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

Class II — Potential Health HazardTerminated
Refund
November 7, 2014· Perry Drug Inc.

Recalled Item: Cyclosporine 0.045 % Sol PF

The Issue: Lack of sterility assurance;All lots of sterile products

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

Class II — Potential Health HazardTerminated
Refund
November 7, 2014· Hospira Inc.

Recalled Item: Sterile powder Vancomycin Hydrochloride for Injection

The Issue: Mislabeling

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

Class III — Low RiskTerminated
Refund
November 7, 2014· Perry Drug Inc.

Recalled Item: Tri-mix Antidote 10 each Syringes

The Issue: Lack of sterility assurance;All lots of sterile products

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

Class II — Potential Health HazardTerminated
Refund
November 7, 2014· Perry Drug Inc.

Recalled Item: Testosterone Cyp 200 mg/mL Sesame Inj.

The Issue: Lack of sterility assurance;All lots of sterile products

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

Class II — Potential Health HazardTerminated
Refund
November 7, 2014· Perry Drug Inc.

Recalled Item: Sodium Tetradecyl SO4 0.3% Inj.

The Issue: Lack of sterility assurance;All lots of sterile products

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

Class II — Potential Health HazardTerminated
Refund
November 3, 2014· REFA Enterprises, LLC

Recalled Item: Forever Beautiful BEE POLLEN

The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found

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

Class I — Serious Health HazardTerminated
Refund
November 3, 2014· REFA Enterprises, LLC

Recalled Item: Forever Beautiful INFINITY

The Issue: Marketed Without an Approved NDA/ANDA: FDA analysis found

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

Class I — Serious Health HazardTerminated
Refund
October 30, 2014· Baxter Healthcare Corp.

Recalled Item: Heparin Sodium in 0.9% Sodium Chloride Injection

The Issue: Subpotent Drug: Heparin raw material was found to

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

Class II — Potential Health HazardTerminated
Refund
October 24, 2014· CareFusion 213, LLC

Recalled Item: Scrub Care Chlorhexidine Gluconate Solution

The Issue: Does Not Meet Monograph: Chlorhexidine Gluconate Surgical Scrub

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

Class III — Low RiskTerminated
Refund
October 24, 2014· Hospira Inc.

Recalled Item: Meropenem I.V. 1 g is supplied in 30 mL injection vials

The Issue: Defective Container: Glass vials may crack due to

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

Class II — Potential Health HazardTerminated
Refund
October 22, 2014· Prometheus Laboratories Inc.

Recalled Item: Mercaptopurine 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 21, 2014· Taro Pharmaceuticals U.S.A., Inc.

Recalled Item: Carbamazepine Tablets USP

The Issue: Marketed without an Approved NDA/ANDA: One lot was

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

Class III — Low RiskTerminated
Refund
October 20, 2014· Nanophase Technologies Corporation

Recalled Item: Z-COTE HP 1 TRANSPARENT ZINC OXIDE

The Issue: cGMP Deviation; The incorrect amount of a raw

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

Class III — Low RiskTerminated
Refund
October 17, 2014· Obagi Medical Products

Recalled Item: Obagi Nu-Derm Clear

The Issue: Labeling: Label Mix-Up; Containers of the Obagi Nu-Derm

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

Class II — Potential Health HazardTerminated
Refund
October 17, 2014· Aurobindo Pharma USA Inc

Recalled Item: Gabapentin Capsules

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
October 16, 2014· Apotex Inc.

Recalled Item: Candesartan Cilexetil Tablets

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
October 16, 2014· Apotex Inc.

Recalled Item: Candesartan Cilexetil Tablets

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund