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 11941–11960 of 17,529 recalls

October 29, 2015· Amerisource Health Services

Recalled Item: HYDROCHLOROTHIAZIDE CAPSULES

The Issue: Presence of Particulate Matter

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

Class II — Potential Health HazardTerminated
Refund
October 29, 2015· PQ Corporation

Recalled Item: EPSOM SALT(Magnesium Sulfate Heptahydrate

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
October 28, 2015· Sanofi-Aventis U.S. LLC

Recalled Item: Auvi-Q (epinephrine injection

The Issue: Defective Delivery System; potential to have inaccurate dosage

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

Class I — Serious Health HazardTerminated
Refund
October 28, 2015· Sanofi-Aventis U.S. LLC

Recalled Item: Auvi-Q (epinephrine injection

The Issue: Defective Delivery System; potential to have inaccurate dosage

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

Class I — Serious Health HazardTerminated
Refund
October 27, 2015· Steris Corp

Recalled Item: Kindest Kare Antimicrobial Foaming Handwash

The Issue: Undeclared Excipients

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

Class II — Potential Health HazardTerminated
Refund
October 27, 2015· Geritrex Corp

Recalled Item: Carbo-O-Philic 40 Gel 40% (Urea) NET WT tube

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined

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

Class II — Potential Health HazardTerminated
Refund
October 27, 2015· Geritrex Corp

Recalled Item: GRx HiCort 25 (hydrocortisone acetate 25 mg) Suppositories

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined

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

Class II — Potential Health HazardTerminated
Refund
October 27, 2015· Geritrex Corp

Recalled Item: Polyethylene Glycol 3350-GRX Powder 100% jars a) 8.4 oz (250

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined

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

Class II — Potential Health HazardTerminated
Refund
October 27, 2015· Geritrex Corp

Recalled Item: Carbo-O-Philic 40 Cream 40% (Urea) tubes

The Issue: Marketed without an Approved NDA/ANDA: FDA has determined

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

Class II — Potential Health HazardTerminated
Refund
October 26, 2015· Par Pharmaceutical Inc.

Recalled Item: Meclizine Hydrochloride Tablets

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
October 26, 2015· Par Pharmaceutical Inc.

Recalled Item: Meclizine Hydrochloride Tablets USP

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund
October 21, 2015· Vintage Pharmaceuticals LLC, DBA Qualitest Pharmaceuticals

Recalled Item: RANITIDINE SYRUP (RANITIDINE ORAL SOLUTION

The Issue: Failed Stability Specifications: Out of Specification results obtained

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

Class III — Low RiskTerminated
Refund
October 21, 2015· Breckenridge Pharmaceutical, Inc

Recalled Item: Duloxetine Delayed-release Capsules

The Issue: Presence of Foreign Tablets/Capsules: one foreign capsule identified

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

Class III — Low RiskTerminated
Refund
October 20, 2015· Teva Pharmaceutical Industries

Recalled Item: Irbesartan and Hydrochlorothiazide tablets USP 150 mg/ 12.5 mg

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
October 19, 2015· Western Drug

Recalled Item: Salicylic Acid Inj

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
October 19, 2015· Western Drug

Recalled Item: Dextrose 50% Inj Sol

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund
October 19, 2015· Oasis Medical, Inc.

Recalled Item: HPMC Visoelastic Topical

The Issue: Failed pH Specification: It has been determined that

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

Class III — Low RiskTerminated
Refund
October 19, 2015· Oasis Medical, Inc.

Recalled Item: HPMC Visoelastic

The Issue: Failed pH Specification: It has been determined that

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

Class III — Low RiskTerminated
Refund
October 19, 2015· Oasis Medical, Inc.

Recalled Item: HPMC Visoelastic

The Issue: Failed pH Specification: It has been determined that

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

Class III — Low RiskTerminated
Refund
October 19, 2015· Western Drug

Recalled Item: Hydroxocobalamin 5000IU/mL Injection

The Issue: Sterility Concerns

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

Class II — Potential Health HazardTerminated
Refund