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 10341–10360 of 17,529 recalls

March 15, 2017· Sun Pharmaceutical Industries, Inc.

Recalled Item: Testosterone Cypionate Injection

The Issue: Presence of Particulate Matter

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

Class II — Potential Health HazardTerminated
Refund
March 13, 2017· Akorn Inc

Recalled Item: Sulfamethoxazole and Trimethoprim Oral Suspension

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
March 13, 2017· Genentech Inc.

Recalled Item: Cotellic (cobimetinib) Tablets

The Issue: Superpotent Drug: An oversized tablet was found in

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

Class II — Potential Health HazardTerminated
Refund
March 12, 2017· Meridian Medical Technologies a Pfizer Company

Recalled Item: EpiPen 2-Pak (Epinephrine) Auto-Injectors 0.3 mg

The Issue: Defective Delivery System; reports of the device failing

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

Class I — Serious Health HazardOngoing
Refund
March 12, 2017· Meridian Medical Technologies a Pfizer Company

Recalled Item: EpiPen Jr. 2-Pak (Epinephrine) Auto-Injectors 0.15 mg

The Issue: Defective Delivery System; reports of the device failing

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

Class I — Serious Health HazardOngoing
Refund
March 10, 2017· Claris Lifesciences Inc

Recalled Item: Fluconazole Injection

The Issue: Lack of Assurance of Sterility: there is potential

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

Class II — Potential Health HazardTerminated
Refund
March 10, 2017· Claris Lifesciences Inc

Recalled Item: Levofloxacin Injection in 5% Dextrose

The Issue: Lack of Assurance of Sterility: there is potential

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

Class II — Potential Health HazardTerminated
Refund
March 10, 2017· Claris Lifesciences Inc

Recalled Item: Ciprofloxacin in Dextrose (5%) Injection

The Issue: Lack of Assurance of Sterility: there is potential

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

Class II — Potential Health HazardTerminated
Refund
March 10, 2017· Claris Lifesciences Inc

Recalled Item: Metronidazole Injection

The Issue: Lack of Assurance of Sterility: there is potential

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

Class II — Potential Health HazardTerminated
Refund
March 8, 2017· Mckesson Medical Surgical

Recalled Item: hydrALAZINE HYDROCHLORIDE INJECTION

The Issue: Temperature Abuse: Certain pieces of these lots distributed

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

Class II — Potential Health HazardTerminated
Refund
March 8, 2017· Isomeric Pharmacy Solution, LLC

Recalled Item: Triamcinolone 40 mg/mL 2 mL Single-Dose Vial for Injection

The Issue: CGMP Deviations

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

Class II — Potential Health HazardTerminated
Refund
March 7, 2017· A&H Focal Inc.

Recalled Item: ZHANSHENG WEIGE CHAOYUE XILISHI tablets

The Issue: Marked 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
March 7, 2017· A&H Focal Inc.

Recalled Item: Ye Lang Shen capsules

The Issue: Marked Without An Approved NDA/ANDA: FDA analysis found

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

Class II — Potential Health HazardTerminated
Refund
March 7, 2017· A&H Focal Inc.

Recalled Item: Zhonghua Niubian tablets

The Issue: Marked 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
March 7, 2017· A&H Focal Inc.

Recalled Item: LANG YI HAO CHAONONGSUOPIAN tablets

The Issue: Marked 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
March 7, 2017· A&H Focal Inc.

Recalled Item: HU HU SHENG WEI capsules

The Issue: Marked 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
March 7, 2017· A&H Focal Inc.

Recalled Item: Indian God Lotion Spray Bottle

The Issue: Marked Without An Approved NDA/ANDA: FDA analysis found

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

Class III — Low RiskTerminated
Refund
March 7, 2017· A&H Focal Inc.

Recalled Item: GERMANY BLACK GOLD tablets

The Issue: Marked 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
March 7, 2017· A&H Focal Inc.

Recalled Item: LIEN CHAN FOR SEVEN DAYS capsules

The Issue: Marked 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
March 7, 2017· A&H Focal Inc.

Recalled Item: Power V8 Viagra tablets

The Issue: Marked 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