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 16421–16440 of 17,529 recalls

May 21, 2013· Baxter Healthcare Corp.

Recalled Item: Heparin Sodium and 0.9% Sodium Chloride Injection

The Issue: Lack of Assurance of Sterility: Specific lot numbers

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

Class II — Potential Health HazardTerminated
Refund
May 21, 2013· Baxter Healthcare Corp.

Recalled Item: 0.9% Sodium Chloride Injection

The Issue: Lack of Assurance of Sterility: Specific lot numbers

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

Class II — Potential Health HazardTerminated
Refund
May 20, 2013· Sandoz Incorporated

Recalled Item: Methotrexate Injection

The Issue: Presence of Particulate Matter: Found during examination of

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

Class I — Serious Health HazardTerminated
Refund
May 20, 2013· Hospira, Inc.

Recalled Item: Ondansetron Injection

The Issue: Presence of Particulate; lot being recalled as a

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

Class II — Potential Health HazardTerminated
Refund
May 20, 2013· Dolphin Intertrade Corporation

Recalled Item: XIYOUJI QINGZHI CAPSULE

The Issue: Undeclared Sibutramine

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

Class I — Serious Health HazardTerminated
Refund
May 20, 2013· Dolphin Intertrade Corporation

Recalled Item: JaDera

The Issue: Undeclared Sibutramine

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

Class I — Serious Health HazardTerminated
Refund
May 17, 2013· Warner Chilcott US LLC

Recalled Item: Enablex (darifenacin) Extended Release Tablet

The Issue: Failed Quality Specifications

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

Class II — Potential Health HazardTerminated
Refund
May 16, 2013· Hospira Inc.

Recalled Item: Diazepam Injection

The Issue: Lack of Assurance of Sterility: Loose crimp applied

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

Class II — Potential Health HazardTerminated
Refund
May 16, 2013· West-Ward Pharmaceutical Corp.

Recalled Item: West-ward Belladonna Alkaloids with Phenobarbital Tablets

The Issue: Presence of Foreign Substance: Belladonna Alkaloids with Phenobarbital

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

Class II — Potential Health HazardTerminated
Refund
May 16, 2013· West-Ward Pharmaceutical Corp.

Recalled Item: West-ward Belladonna Alkaloids with Phenobarbital Tablets

The Issue: Cross contamination with other products: Belladonna Alkaloids with

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

Class II — Potential Health HazardTerminated
Refund
May 15, 2013· Novartis Consumer Health

Recalled Item: Theraflu Warming Relief

The Issue: Failed Impurities/Degradation:Specifications:Unknown degradant found during stab

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

Class III — Low RiskTerminated
Refund
May 15, 2013· Novartis Consumer Health

Recalled Item: Maximum Strength Comtrex Nighttime Cold & Cough

The Issue: Failed Impurities/Degradation:Specifications:Unknown degradant found during stab

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

Class III — Low RiskTerminated
Refund
May 15, 2013· Novartis Consumer Health

Recalled Item: Maximum Strength Comtrex

The Issue: Failed Impurities/Degradation:Specifications:Unknown degradant found during stab

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

Class III — Low RiskTerminated
Refund
May 15, 2013· Novartis Consumer Health

Recalled Item: Maximum Strength Comtrex

The Issue: Failed Impurities/Degradation:Specifications:Unknown degradant found during stab

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

Class III — Low RiskTerminated
Refund
May 15, 2013· Health & Beyond

Recalled Item: HEALTH & BEYOND DR. LARRY'S Tranquility DIETARY SUPPLEMENT 30 Capsules

The Issue: Marketed Without an Approved NDA/ANDA; product found to

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

Class II — Potential Health HazardTerminated
Refund
May 15, 2013· Actavis South Atlantic LLC

Recalled Item: Ranitidine Syrup (Ranitidine Oral Solution USP) 15 mg/mL

The Issue: Failed Impurity/Degradation Specification; "Related Compound C"

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

Class II — Potential Health HazardTerminated
Refund
May 15, 2013· Pentec Health

Recalled Item: Proplete 90+ KG (Intraperitoneal Parenteral Nutrition - dialysate solution with

The Issue: Lack of Assurance of Sterility: Sterility could not

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

Class II — Potential Health HazardTerminated
Refund
May 15, 2013· Pentec Health

Recalled Item: Baxter LL bag 2% Amino Acids (Intraperitoneal Parenteral Nutrition -

The Issue: Lack of Assurance of Sterility: Sterility could not

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

Class II — Potential Health HazardTerminated
Refund
May 15, 2013· Pentec Health

Recalled Item: Proplete 45 - 51 KG (Intraperitoneal Parenteral Nutrition - dialysate

The Issue: Lack of Assurance of Sterility: Sterility could not

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

Class II — Potential Health HazardTerminated
Refund
May 15, 2013· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Budesonide Capsules

The Issue: Failed Quality Specifications

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

Class III — Low RiskTerminated
Refund