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 4321–4340 of 17,529 recalls
Recalled Item: Irbesartan Tablets USP
The Issue: CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irbesartan Tablets USP
The Issue: CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methocarbamol 500mg Tablet
The Issue: Labeling: Label Error on Declared Strength; Bottles labeled
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irbesartan and Hydrochlorothiazide Tablets USP
The Issue: CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AllerClear D-24 hr
The Issue: Failed Moisture Limits
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Loratadine-D Extended-Release Tablets (Loratadine and Pseudoephedrine Sulfate
The Issue: Failed Moisture Limits
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Imipramine Pamoate Capsules 125 mg
The Issue: Out of specification result observed in a dissolution
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cetirizine hydrochloride
The Issue: Labeling: Not Elsewhere classified: Product was relabeled as
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dr. Reddy's Ezetimibe and Simvastatin Tablets
The Issue: Failed Excipient Specifications; product manufactured using an excipient
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dr. Reddy's Ezetimibe and Simvastatin Tablets
The Issue: Failed Excipient Specifications; product manufactured using an excipient
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dr. Reddy's Ezetimibe and Simvastatin Tablets
The Issue: Failed Excipient Specifications; product manufactured using an excipient
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dr. Reddy's Ezetimibe and Simvastatin Tablets
The Issue: Failed Excipient Specifications and Presence of Foreign Tablets/Capsules;
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dr. Reddy's Ezetimibe and Simvastatin Tablets
The Issue: Failed Excipient Specifications; product manufactured using an excipient
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Omeprazole Delayed-Release Capsules
The Issue: CGMP Deviations: Customer complaint for the presence of
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Betaxolol Ophthalmic Solution
The Issue: Microbial Contamination of Sterile Products: Confirmed sterility failure
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tinactin (Tolnaftate 1%) POWDER SPRAY NET WT 133g (4.6 oz) can
The Issue: Chemical Contamination: presence of benzene
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tinactin (Tolnaftate 1%) LIQUID SPRAY NET WT150g (5.3 OZ) can
The Issue: Chemical Contamination: presence of benzene
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tinactin (Tolnaftate 1%) DEODORANT POWDER SPRAY NET WT 133g (4.6 OZ) can
The Issue: cGMP Deviations: manufactured at the same facility where
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LOTRIMIN AF
The Issue: Chemical Contamination: presence of benzene
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LOTRIMIN AF (Miconazole nitrate 2%) Deodorant Powder Spray NET WT
The Issue: cGMP Deviations: manufactured at the same facility where
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.