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 10961–10980 of 17,529 recalls

September 19, 2016· Wells Pharmacy Network, LLC

Recalled Item: Testosterone 200 mg/Anastrazole 20mg Pellet

The Issue: Superpotent and Subpotent drugs

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

Class II — Potential Health HazardTerminated
Refund
September 19, 2016· Wells Pharmacy Network, LLC

Recalled Item: Testosterone 60 mg/Anastrazole 4 mg Pellet

The Issue: Superpotent and Subpotent drugs

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

Class II — Potential Health HazardTerminated
Refund
September 19, 2016· Wells Pharmacy Network, LLC

Recalled Item: Testosterone 200 mg/Anastrozole 9 mg Pellet

The Issue: Superpotent and Subpotent drugs

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

Class II — Potential Health HazardTerminated
Refund
September 19, 2016· Wells Pharmacy Network, LLC

Recalled Item: Estradiol 12.5 mg Pellet

The Issue: Superpotent and Subpotent drugs

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

Class III — Low RiskTerminated
Refund
September 19, 2016· Wells Pharmacy Network, LLC

Recalled Item: Estradiol 3 mg Pellet

The Issue: Superpotent and Subpotent drugs

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

Class III — Low RiskTerminated
Refund
September 16, 2016· Hospira Inc., A Pfizer Company

Recalled Item: Marcaine 0.25% (bupivacaine HCl) injection

The Issue: Lack of Assurance of Sterility and Subpotent Drug:

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

Class II — Potential Health HazardTerminated
Refund
September 16, 2016· Hospira Inc., A Pfizer Company

Recalled Item: Marcaine 0.5% (bupivacaine HCl) injection

The Issue: Lack of Assurance of Sterility and Subpotent Drug:

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

Class II — Potential Health HazardTerminated
Refund
September 15, 2016· Pfizer Inc.

Recalled Item: PREMARIN (conjugated estrogen tablets

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

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

Class III — Low RiskTerminated
Refund
September 15, 2016· Mckesson Packaging Services

Recalled Item: Xanax (Alprazolam) USP

The Issue: Labeling: Missing Label-Primary packaging label (i.e. blister card)

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

Class III — Low RiskTerminated
Refund
September 13, 2016· Taro Pharmaceuticals, Inc.

Recalled Item: Desoximetasone Cream USP

The Issue: Failed Stability Specifications: The subject lots exhibited OOS

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

Class II — Potential Health HazardTerminated
Refund
September 13, 2016· Teva Pharmaceuticals USA

Recalled Item: mitoXANTRONE Injection USP (concentrate)

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
September 13, 2016· Sun Pharmaceutical Industries, Inc.

Recalled Item: buPROPion Hydrochloride Extended-release Tablets

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
September 13, 2016· Taro Pharmaceuticals, Inc.

Recalled Item: Desoximetasone Cream USP

The Issue: Failed Stability Specifications: The subject lots exhibited OOS

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

Class II — Potential Health HazardTerminated
Refund
September 12, 2016· The Apothecary Shoppe LLC

Recalled Item: Phenotolamine 0.4mg/Prostaglandin 20mcg/mL packaged in 2.5 mL sterile vials

The Issue: Lack of Assurance of Sterility; medication was sterilized

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

Class II — Potential Health HazardTerminated
Refund
September 12, 2016· The Apothecary Shoppe LLC

Recalled Item: Tri-Mix 18/1/10 (Papaverine 18mg

The Issue: Lack of Assurance of Sterility; medication was sterilized

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

Class II — Potential Health HazardTerminated
Refund
September 12, 2016· MOORE'S COMPOUNDING PHARMACY

Recalled Item: Levothyroxine Sodium 135 mcg/Liothyronine 15 mcg SR capsules

The Issue: Superpotent Drug and Subpotent Drug; potency failures obtained

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

Class II — Potential Health HazardTerminated
Refund
September 12, 2016· The Apothecary Shoppe LLC

Recalled Item: Methylcobalamin 5000 mcg/mL Injection

The Issue: Lack of Assurance of Sterility; medication was sterilized

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

Class II — Potential Health HazardTerminated
Refund
September 9, 2016· Pfizer Inc.

Recalled Item: Cytotec (misoprostol) Tablets

The Issue: Failed Impurities/Degradations Specifications; Out of specification results for

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

Class III — Low RiskTerminated
Refund
September 9, 2016· Cadila Pharmaceuticals Limited

Recalled Item: Ondansetron HCI API

The Issue: Microbial Contamination of Non-Sterile Product

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

Class II — Potential Health HazardTerminated
Refund
September 8, 2016· Mckesson Packaging Services

Recalled Item: Lansoprazole Delayed-Release Capsules

The Issue: Mislabeling

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

Class III — Low RiskTerminated
Refund