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 16961–16980 of 17,529 recalls

December 21, 2012· Warner Chilcott Company LLC

Recalled Item: Femtrace 0.45 mg (Estradiol Acetate) Tablets

The Issue: Failed Impurity/Degradation Specifications due to moisture ingress in

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

Class III — Low RiskTerminated
Refund
December 21, 2012· Lee Pharmaceuticals, Inc

Recalled Item: 12-Hour Sinus (oxymetazoline hydrochloride) Nasal Spray

The Issue: Microbial Contamination of a Non-Sterile Products: 12-Hour Sinus

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

Class II — Potential Health HazardTerminated
Refund
December 19, 2012· P & J Trading Co

Recalled Item: SLIMDIA Revolution capsules

The Issue: Marketed Without an Approved NDA/ANDA: All lots of

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

Class I — Serious Health HazardTerminated
Refund
December 18, 2012· Matrixx Initiatives Inc

Recalled Item: Zicam Extreme Congestion Relief (oxymetazoline HCl) nasal gel

The Issue: Microbial Contamination of Non-Sterile Products: Product may be

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

Class I — Serious Health HazardTerminated
Refund
December 18, 2012· Belmora LLC

Recalled Item: Flanax (aluminum hydroxide

The Issue: Defective Container: Product lacks tamper evident breakaway band

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

Class III — Low RiskTerminated
Refund
December 18, 2012· Watson Pharmaceuticals

Recalled Item: Taztia XT(diltiazem HCI extended release capsules

The Issue: Failed Dissolution Specification: Out of a specification result

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

Class II — Potential Health HazardTerminated
Refund
December 17, 2012· Pacira Pharmaceuticals, Inc.

Recalled Item: EXPAREL (bupivacaine liposome injectable suspension)

The Issue: Subpotent; bupivacaine

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

Class II — Potential Health HazardTerminated
Refund
December 17, 2012· L. Perrigo Co.

Recalled Item: Prednisone tablets

The Issue: Presence of Foreign Substance(s); Perrigo has been notified

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

Class II — Potential Health HazardTerminated
Refund
December 17, 2012· Performance Plus Marketing, Inc.

Recalled Item: Mojo nights SUPREME Capsules

The Issue: Undeclared Sildenafil

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

Class I — Serious Health HazardTerminated
Refund
December 17, 2012· Performance Plus Marketing, Inc.

Recalled Item: libigrow capsules

The Issue: Undeclared Sildenafil

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

Class I — Serious Health HazardTerminated
Refund
December 17, 2012· Performance Plus Marketing, Inc.

Recalled Item: libigrow XXXTREME Capsules

The Issue: Undeclared Sildenafil

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

Class I — Serious Health HazardTerminated
Refund
December 17, 2012· Performance Plus Marketing, Inc.

Recalled Item: CASANOVA Capsules

The Issue: Undeclared Sildenafil

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

Class I — Serious Health HazardTerminated
Refund
December 17, 2012· Performance Plus Marketing, Inc.

Recalled Item: BLUE Diamond Pill

The Issue: Undeclared Sildenafil

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

Class I — Serious Health HazardTerminated
Refund
December 17, 2012· Performance Plus Marketing, Inc.

Recalled Item: BLUE Diamond PLATINUM Capsules

The Issue: Undeclared Sildenafil

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

Class I — Serious Health HazardTerminated
Refund
December 17, 2012· Performance Plus Marketing, Inc.

Recalled Item: Mojo nights Capsules

The Issue: Undeclared Sildenafil

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

Class I — Serious Health HazardTerminated
Refund
December 14, 2012· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Hydrocodone Bitartrate and Acetaminophen Tablets

The Issue: Superpotent (Multiple Ingredient) Drug: Oversized tablets resulting in

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

Class I — Serious Health HazardTerminated
Refund
December 13, 2012· Watson Laboratories Inc

Recalled Item: Caziant (desogestrel and ethinyl estradiol) Tablets

The Issue: Impurities/Degradation Products: Out-of-specification results were obtained for

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

Class III — Low RiskTerminated
Refund
December 12, 2012· Boehringer Ingelheim Roxane Inc

Recalled Item: Perindopril Erbumine Tablets

The Issue: Impurities/Degradation Products: Out of Specification results found for

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

Class III — Low RiskTerminated
Refund
December 12, 2012· Schering-Plough Products, LLC

Recalled Item: Temodar (temozolomide) Capsule

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
December 10, 2012· Upsher Smith Laboratories, Inc.

Recalled Item: Divalproex Sodium Delayed-Release Tablets

The Issue: Labeling: Label Error On Declared Strength; Some bottles

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

Class III — Low RiskTerminated
Refund