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 17081–17100 of 17,529 recalls

September 21, 2012· Baxter Healthcare Corp.

Recalled Item: 5% Dextrose and 0.45% Sodium Chloride Injection USP

The Issue: Chemical Contamination: The IV solutions were packaged in

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

Class II — Potential Health HazardTerminated
Refund
September 21, 2012· American Enterprises LLC dba Sterling Gelatin

Recalled Item: Limed Bone Gelatin

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 21, 2012· Baxter Healthcare Corp.

Recalled Item: 0.9% Sodium Chloride Injection USP

The Issue: Chemical Contamination: The IV solutions were packaged in

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

Class II — Potential Health HazardTerminated
Refund
September 21, 2012· Watson Laboratories Inc

Recalled Item: Hydrocodone Bitartrate and Acetaminophen Tablets USP

The Issue: Superpotent (Multiple Ingredient) Drug: There is the potential

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

Class I — Serious Health HazardTerminated
Refund
September 21, 2012· Baxter Healthcare Corp.

Recalled Item: 5% Dextrose Injection USP

The Issue: Chemical Contamination: The IV solutions were packaged in

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

Class II — Potential Health HazardTerminated
Refund
September 20, 2012· Genentech Inc

Recalled Item: Nutropin AQ NuSpin 20 (somatropin (rDNA origin) injection} 20 mg/ 2mL Genentech

The Issue: Miscalibrated and/or Defective Delivery System: Genentech has received

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

Class II — Potential Health HazardTerminated
Refund
September 20, 2012· Globe All Wellness, LLC

Recalled Item: SLIM XTREME Herbal Slimming Capsule

The Issue: Marketed Without an Approved NDA/ANDA: Product tested positive

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

Class I — Serious Health HazardTerminated
Refund
September 20, 2012· Genentech Inc

Recalled Item: Nutropin AQ NuSpin 10 (somatropin (rDNA origin) injection} 10 mg/ 2mL Genentech

The Issue: Miscalibrated and/or Defective Delivery System: Genentech has received

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

Class II — Potential Health HazardTerminated
Refund
September 20, 2012· Sandoz Incorporated

Recalled Item: Children's Cetirizine HCl Chewable Tablets 5 mg

The Issue: Impurity/Degradation; exceeded impurity specification at the 8 and

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

Class III — Low RiskTerminated
Refund
September 17, 2012· DermaCare, Inc.

Recalled Item: UP & UP brand

The Issue: Microbial Contamination of Non-Sterile Products: Laboratory findings of

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

Class II — Potential Health HazardTerminated
Refund
September 17, 2012· DermaCare, Inc.

Recalled Item: UP & UP brand

The Issue: Microbial Contamination of Non-Sterile Products: Laboratory findings of

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

Class II — Potential Health HazardTerminated
Refund
September 12, 2012· Sandoz Incorporated

Recalled Item: Pramipexole Dihydrochloride Tablets

The Issue: Impurities/Degradation Products: An out of specification result for

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

Class III — Low RiskTerminated
Refund
September 12, 2012· Sandoz Incorporated

Recalled Item: Pramipexole Dihydrochloride Tablets

The Issue: Impurities/Degradation Products: An out of specification result for

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

Class III — Low RiskTerminated
Refund
September 10, 2012· Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals

Recalled Item: HYDROCODONE BITARTRATE and ACETAMINOPHEN TABLETS

The Issue: Superpotent (Multiple Ingredient) Drug: Confirmed customer complaints of

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

Class I — Serious Health HazardOngoing
Refund
September 6, 2012· Church & Dwight Inc

Recalled Item: Orajel Kids My Way! Anticavity Fluoride (sodium fluoride) toothpaste

The Issue: CGMP Deviations: Product was made with an incorrect

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

Class II — Potential Health HazardTerminated
Refund
September 5, 2012· F. Hoffmann-LaRoche Ltd.

Recalled Item: Cymevene 500 mg Powder for Infusion

The Issue: Lack of Assurance of Sterility; container closure issues

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: Berkley & Jensen 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 Plus Calcium 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: Best Choice Health Care

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: CVS Pharmacy Fiber Capsules for Regularity

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