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 17481–17500 of 17,529 recalls

February 23, 2012· www.vitaminbestbuy.com

Recalled Item: Man King Capsules

The Issue: Marketed Without an Approved ANDA/NDA: presence of sildenafil

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

Class I — Serious Health HazardTerminated
Refund
February 20, 2012· Physicians Total Care, Inc.

Recalled Item: PHYSICIANS TOTAL CARE

The Issue: Presence of Foreign Substance(s): There is a potential

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

Class II — Potential Health HazardTerminated
Refund
February 20, 2012· Physicians Total Care, Inc.

Recalled Item: PHYSICIANS TOTAL CARE

The Issue: Presence of Foreign Substance(s): There is a potential

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

Class II — Potential Health HazardTerminated
Refund
February 8, 2012· Physicians Total Care, Inc.

Recalled Item: Lipitor (Atorvastatin calcium)

The Issue: Chemical Contamination: Complaints of an uncharacteristic odor identified

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

Class II — Potential Health HazardTerminated
Refund
February 6, 2012· sanofi-aventis US, Inc.

Recalled Item: Eloxatin (OXALIplatin injection) 5 mg/mL Injection

The Issue: CGMP Deviations: Eloxatin was manufactured by Ben Venue

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

Class II — Potential Health HazardTerminated
Refund
February 6, 2012· sanofi-aventis US, Inc.

Recalled Item: Eloxatin (OXALIplatin injection) 5 mg/mL injection

The Issue: CGMP Deviations: Eloxatin was manufactured by Ben Venue

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

Class II — Potential Health HazardTerminated
Refund
February 3, 2012· Lloyd Inc

Recalled Item: Thyro-Tab 0.050mg.

The Issue: Subpotent (Single Ingredient Drug): Low assay at the

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

Class II — Potential Health HazardTerminated
Refund
February 3, 2012· Lloyd Inc

Recalled Item: Levothroid (levothyroxine sodium tablets

The Issue: Subpotent (Single Ingredient Drug): Low assay at the

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

Class II — Potential Health HazardTerminated
Refund
December 19, 2011· Body Basics Inc

Recalled Item: Actra-SX 500 Capsules

The Issue: Marketed without an Approved NDA/ANDA; product contains sildenafil,

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

Class I — Serious Health HazardTerminated
Refund
December 2, 2011· Eagle Pharmaceuticals Inc.

Recalled Item: Argatroban Injection 50 mg per 50ml (1 mg per ml) For Intravenous Infusion Only

The Issue: A complaint was received from a hospital pharmacy

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

Class I — Serious Health HazardTerminated
Refund
November 10, 2011· Victus, Inc.

Recalled Item: Hipoglos Ointment (zinc oxide and lanolin)

The Issue: Misbranded

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

Class II — Potential Health HazardTerminated
Refund
November 8, 2011· Carefusion 213, Llc

Recalled Item: ChloraPrep with Tint

The Issue: Lack of Assurance of Sterility: A customer complaint

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

Class II — Potential Health HazardTerminated
Refund
October 17, 2011· Meda Pharmaceuticals Inc.

Recalled Item: Prefera OB One Gel Capsules

The Issue: Undeclared Color

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

Class II — Potential Health HazardTerminated
Refund
September 30, 2011· VistaPharm, Inc.

Recalled Item: Xactdose Phenytoin Oral Suspension

The Issue: Defective container; lidding deformity allows the contained product

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

Class II — Potential Health HazardTerminated
Refund
September 27, 2011· Shamrock Medical Solutions Group LLC

Recalled Item: Pramipexole Dihydrochloride Tablets

The Issue: Labeling: Label Mix up; product labeled to contain

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

Class II — Potential Health HazardTerminated
Refund
September 27, 2011· Shamrock Medical Solutions Group LLC

Recalled Item: Docusate Calcium Softgel Capsules

The Issue: Labeling: Label Mix up; product labeled to contain

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

Class II — Potential Health HazardTerminated
Refund
September 27, 2011· Shamrock Medical Solutions Group LLC

Recalled Item: metFORMIN ER Tablets

The Issue: Labeling: Label Mix up; product labeled did not

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

Class I — Serious Health HazardTerminated
Refund
September 27, 2011· Shamrock Medical Solutions Group LLC

Recalled Item: Oxycodone HCl Oral Concentrate

The Issue: Labeling: Label Mix up; product labeled as Morphine

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

Class I — Serious Health HazardTerminated
Refund
September 27, 2011· Shamrock Medical Solutions Group LLC

Recalled Item: Taztia XT (Diltiazem HCl) Capsules

The Issue: Labeling: Label Mix Up; packages labeled as Thiamine

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

Class I — Serious Health HazardTerminated
Refund
September 27, 2011· Shamrock Medical Solutions Group LLC

Recalled Item: Sulfamethoxazole and Trimethoprim Tablets

The Issue: Labeling: Label Mix up; product labeled to contain

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

Class II — Potential Health HazardTerminated
Refund