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 13301–13320 of 17,529 recalls
Recalled Item: Lansoprazole Delayed-Release Capsules
The Issue: CGMP Deviations: Firm did not adequately investigate customer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zonisamide Capsules
The Issue: CGMP Deviations: Firm did not adequately investigate customer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amlodipine Besylate Tablets
The Issue: CGMP Deviations: Firm did not adequately investigate customer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Captopril Tablets
The Issue: CGMP Deviations: Firm did not adequately investigate customer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metoprolol Succinate Extended-Release Tablets
The Issue: CGMP Deviations: Firm did not adequately investigate customer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisinopril Tablets USP
The Issue: CGMP Deviations: Firm did not adequately investigate customer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Famotodine Tablets
The Issue: CGMP Deviations: Firm did not adequately investigate customer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisinopril Tablets USP
The Issue: CGMP Deviations: Firm did not adequately investigate customer
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NITROFURANTOIN MONOHYDRATE/MACROCRYSTALS CAPSULES
The Issue: Failed Dissolution Specification; 6 month time point
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IC-GREEN (indocyanine green for injection
The Issue: Subpotent Drug: Low out-of-specification potency result of the
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chlordiazepoxide HCl/Clidinium Bromide capsules
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Librax (5 mg chlordiazepoxide HCl and 2.5 mg clidinium bromide) capsules
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nifedipine Extended-Release Tablets
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Well at Walgreens Regular Strength Antacid Liquid
The Issue: Products failed the Antimicrobial Effectiveness Test
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Well at Walgreens Maximum Strength Comfort Gel 12 FL OZ (355 mL) bottle
The Issue: Products failed the Antimicrobial Effectiveness Test
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Well at Walgreens Regular Strength Comfort Gel Cherry Flavor
The Issue: Products failed the Antimicrobial Effectiveness Test
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mucinex Fast Max Day Time Severe Cold and Fast-Max Night
The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mucinex Fast Max Severe Congestion & Cough
The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mucinex Fast Max DM Max
The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mucinex Fast Max Night Time Cold & Flu
The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.