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 17101–17120 of 17,529 recalls

September 4, 2012· Raritan Pharmaceuticals, Inc.

Recalled Item: Simply Right Healthcare Fiber Capsules

The Issue: Microbial Contamination of Non-Sterile Products: Product is being

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

Class II — Potential Health HazardTerminated
Refund
September 4, 2012· Raritan Pharmaceuticals, Inc.

Recalled Item: Up&Up Psyllium Fiber Supplement

The Issue: Microbial Contamination of Non-Sterile Products: Product is being

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

Class II — Potential Health HazardTerminated
Refund
September 4, 2012· Raritan Pharmaceuticals, Inc.

Recalled Item: DRxChoice Fiber Capsules

The Issue: Microbial Contamination of Non-Sterile Products: Product is being

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

Class II — Potential Health HazardTerminated
Refund
September 4, 2012· Raritan Pharmaceuticals, Inc.

Recalled Item: Premier Value Fiber Plus Calcium Supplement Capsules

The Issue: Microbial Contamination of Non-Sterile Products: Product is being

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

Class II — Potential Health HazardTerminated
Refund
September 4, 2012· Apace KY LLC

Recalled Item: Enalapril Maleate Tablet

The Issue: Labeling Illegible: Some bottles labels have incomplete NDC

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

Class III — Low RiskTerminated
Refund
September 4, 2012· Raritan Pharmaceuticals, Inc.

Recalled Item: Premier Value Fiber Capsules

The Issue: Microbial Contamination of Non-Sterile Products: Product is being

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

Class II — Potential Health HazardTerminated
Refund
September 4, 2012· Raritan Pharmaceuticals, Inc.

Recalled Item: Leader Fiber Capsules

The Issue: Microbial Contamination of Non-Sterile Products: Product is being

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

Class II — Potential Health HazardTerminated
Refund
September 4, 2012· Raritan Pharmaceuticals, Inc.

Recalled Item: Wal-Mucil 100% Natural Fiber

The Issue: Microbial Contamination of Non-Sterile Products: Product is being

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

Class II — Potential Health HazardTerminated
Refund
September 4, 2012· Raritan Pharmaceuticals, Inc.

Recalled Item: Equate Fiber Therapy

The Issue: Microbial Contamination of Non-Sterile Products: Product is being

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

Class II — Potential Health HazardTerminated
Refund
August 31, 2012· Hospira Inc.

Recalled Item: 0.9% Sodium Chloride Injection

The Issue: Presence of Particulate Matter; product may contain fibrous

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

Class I — Serious Health HazardTerminated
Refund
August 29, 2012· Bristol-myers Squibb Company

Recalled Item: BiCNU (Carmustine for injection) 100 mg and Diluent Rx Only

The Issue: Superpotent (Single Ingredient) Drug: All BiCNU lots within

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

Class I — Serious Health HazardTerminated
Refund
August 29, 2012· Hospira Inc.

Recalled Item: Propofol Injectable Emulsion

The Issue: Presence of Particulate Matter: A single visible particulate

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

Class II — Potential Health HazardTerminated
Refund
August 28, 2012· Dispensing Solutions, Inc

Recalled Item: Atrovent HFA Inhalation Aerosol

The Issue: Label Mix up; side panel of sticker label

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

Class II — Potential Health HazardTerminated
Refund
August 28, 2012· James G. Cole, Inc.

Recalled Item: I-C Drops

The Issue: Lack of Assurance of Sterility: The product is

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

Class II — Potential Health HazardTerminated
Refund
August 28, 2012· 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
August 28, 2012· Hospira Inc.

Recalled Item: Preservative-Free MORPHINE Sulfate 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
August 27, 2012· Samantha Lynn, Inc

Recalled Item: Reumofan Plus Tablets

The Issue: Undeclared Drug

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

Class I — Serious Health HazardTerminated
Refund
August 23, 2012· Stat Rx USA

Recalled Item: Venlafaxine ER 150mg

The Issue: Labeling: Label Mix-up: Product was incorrectly labeled,"Tabs" instead

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

Class III — Low RiskTerminated
Refund
August 23, 2012· Ferring Pharmaceuticals Inc

Recalled Item: Novarel¿ (Chorionic Gonadotropin for injection

The Issue: Labeling; incorrect or missing insert; Warnings portion of

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

Class III — Low RiskTerminated
Refund
August 23, 2012· Evol Nutrition

Recalled Item: Mojo Nights for Her

The Issue: Marketed Without an Approved NDA/ANDA: The products were

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

Class I — Serious Health HazardTerminated
Refund