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 8901–8920 of 17,529 recalls

July 13, 2018· Prinston Pharmaceutical Inc

Recalled Item: Solco Healthcare US Valsartan and Hydrochlorothiazide

The Issue: CGMP Deviations: Carcinogen impurity detected in API used

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

Class II — Potential Health HazardOngoing
Refund
July 13, 2018· Prinston Pharmaceutical Inc

Recalled Item: Solco Healthcare US Valsartan and Hydrochlorothiazide

The Issue: CGMP Deviations: Carcinogen impurity detected in API used

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

Class II — Potential Health HazardOngoing
Refund
July 13, 2018· Prinston Pharmaceutical Inc

Recalled Item: Solco Healthcare US Valsartan and Hydrochlorothiazide

The Issue: CGMP Deviations: Carcinogen impurity detected in API used

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

Class II — Potential Health HazardOngoing
Refund
July 12, 2018· Sun Pharmaceutical Industries, Inc.

Recalled Item: Testosterone Cypionate Injection

The Issue: Presence of Particulate Matter: organic and inorganic compounds

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

Class II — Potential Health HazardTerminated
Refund
July 11, 2018· Renaissance Lakewood, LLC

Recalled Item: Fluconazole Injection

The Issue: Superpotent Drug: lots out of specification for elevated

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

Class III — Low RiskTerminated
Refund
July 11, 2018· Renaissance Lakewood, LLC

Recalled Item: Fluconazole Injection

The Issue: Superpotent Drug and Failed Stability Specifications: lot out

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

Class III — Low RiskTerminated
Refund
July 11, 2018· Renaissance Lakewood, LLC

Recalled Item: Fluconazole Injection

The Issue: Failed Stability Specifications: lot out of specification for

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

Class III — Low RiskTerminated
Refund
July 10, 2018· Valeant Pharmaceuticals North America LLC

Recalled Item: Diazepam Rectal Gel

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
July 9, 2018· Mylan Pharmaceuticals Inc.

Recalled Item: Triamterene and Hydrochlorothiazide Tablets

The Issue: Subpotent Drug

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

Class III — Low RiskTerminated
Refund
July 5, 2018· The Hain Celestial Group, Inc. - Worldwide HQ

Recalled Item: alba BOTANICA sport mineral sunscreen (titanium dioxide 7.0% and zinc

The Issue: Incorrect Product Formulation: wrong sunscreen product in the

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

Class II — Potential Health HazardTerminated
Refund
July 5, 2018· Sanofi-Aventis U.S. LLC

Recalled Item: Admelog Solostar (insulin lispro injection)

The Issue: Temperature Abuse: Product samples of Admelog may not

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

Class II — Potential Health HazardOngoing
Refund
July 5, 2018· Teva Pharmaceuticals USA

Recalled Item: Fluocinolone Acetonide Topical Solution

The Issue: Failed Impurities and Degradation Specifications and Subpotent Drug:

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

Class II — Potential Health HazardTerminated
Refund
July 3, 2018· Sun Pharmaceutical Industries, Inc.

Recalled Item: Metformin Hydrochloride Extended Release Tablets

The Issue: Presence of foreign substance: One lot fo Metformin

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

Class II — Potential Health HazardTerminated
Refund
July 3, 2018· Medgyn Products, Inc.

Recalled Item: Monsel's Solution (Ferric Subsulfate)

The Issue: CGMP Deviations: The manufacturer of this product recalled

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

Class II — Potential Health HazardTerminated
Refund
July 3, 2018· Medi-Fare Drug and Home Health Center

Recalled Item: Potassium Chloride For Injection Concentrate syringe 40 mEq/20 mL (2 mEq/mL)

The Issue: CGMP Deviations: Syringes were filled with 19mL of

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

Class II — Potential Health HazardTerminated
Refund
July 2, 2018· AuroMedics Pharma LLC

Recalled Item: Piperacillin and Tazobactam for Injection USP 3.375 grams per vial

The Issue: Presence of Particulate Matter: identified as glass and

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

Class I — Serious Health HazardTerminated
Refund
June 29, 2018· SCA Pharmaceuticals

Recalled Item: Buffered Lidocaine 1% with Sodium Bicarbonate Injection for Local Anesthetic

The Issue: Subpotent Drug: Stability data does not support the

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

Class II — Potential Health HazardTerminated
Refund
June 29, 2018· Fagron Compounding Services LLC dba Fagron Sterile Services

Recalled Item: Neostigmine Methylsulfate Injection Solution

The Issue: Labeling: Label Error on Declared Strength: syringes of

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

Class I — Serious Health HazardTerminated
Refund
June 29, 2018· Fagron Compounding Services LLC dba Fagron Sterile Services

Recalled Item: Neostigmine Methylsulfate Injection Solution

The Issue: Labeling: Label Error on Declared Strength: syringes of

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

Class I — Serious Health HazardTerminated
Refund
June 28, 2018· PFIZER

Recalled Item: Daptomycin for Injection

The Issue: Microbial Contamination of Sterile Products: Product associated with

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

Class II — Potential Health HazardTerminated
Refund