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.
Showing 7981–8000 of 17,529 recalls
Recalled Item: Isosorbide Dinitrate Tablets
The Issue: Cross Contamination with Other Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Isosorbide Dinitrate Tablets
The Issue: Cross Contamination with Other Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Isosorbide Dinitrate Tablets
The Issue: Cross Contamination with Other Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Isosorbide Dinitrate Tablets
The Issue: Cross Contamination with Other Products
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: curaplex Epi Safe Administration and Training Kits # 8600-01100. Kit
The Issue: Labeling: Incorrect or Missing Lot and/or Exp date:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Curaplex Epi Safe Kit
The Issue: Labeling: Incorrect or missing Lot and/or Exp Date:The
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sandoz Losartan Potassium and Hydrochlorothiazide Tablets
The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BEVACIZUMAB 2.5 MG/0.1ML
The Issue: Sterility Concerns
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Omnipaque (iohexol) Injection
The Issue: Defective Container: vial defect was identified that could
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Westminster Irbesartan Tablets
The Issue: CGMP Deviations: FDA laboratory testing confirmed traces of
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Westminster Irbesartan Tablets
The Issue: CGMP Deviations: FDA laboratory testing confirmed traces of
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Westminster Irbesartan Tablets
The Issue: CGMP Deviations: FDA laboratory testing confirmed traces of
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clindamycin Phosphate Topical Solution USP
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Westminister Irbesartan Tablets
The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GSMS Irbesartan Tablets
The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Westminister Irbesartan Tablets
The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GSMS Irbesartan Tablets
The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GSMS Irbesartan Tablets
The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Westminister Irbesartan Tablets
The Issue: CGMP Deviations: FDA laboratory testing confirmed presence of
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levetiracetam in 0.54 % Sodium Chloride Injection 1
The Issue: Labeling: Label Error on Declared Strength; the pre-printed
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.