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 5861–5880 of 17,529 recalls
Recalled Item: *Morphine 2 mg/mL Cassette
The Issue: Lack of Assurance of Sterility: due to concerns
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Doxycycline Capsules
The Issue: CGMP Deviations: Doxycycline capsules were not manufactured under
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Doxycycline Capsules
The Issue: CGMP Deviations: Doxycycline capsules were not manufactured under
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pantoprazole Sodium Delayed-Release Tablets
The Issue: CGMP Deviations: Presence of dark brown discoloration on
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Buprexone Banana cream 6-0.6 mg Troche
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Buprenorphine Black Cherry 2 mg Troche
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Buprenorphine Watermelon 8 mg Troche
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sotalol HCL Tablets
The Issue: Presence of particulate matter. presence of metal particles
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atorvastatin Calcium Tablets
The Issue: Presence of foreign substance: Foreign matter has been
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levonorgestrel and Ethinyl Estradiol Tablets USP
The Issue: Failed Content Uniformity Specifications: Out Of Specification test
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bekyree (desogestrel and ethinyl estradiol tablets USP
The Issue: Failed Content Uniformity Specifications: Out Of Specification test
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Theophylline (Anhydrous) Extended-Release Tablets
The Issue: CGMP Deviations: poor manufacturing practices resulted in Labeling:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acetaminophen 500 mg tablet packaged in a) 30-count bottles ( NDC 52959-0002-30)
The Issue: Presence of Foreign Tablets/Capsules: Complaint involving one Women's
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Epinephrine Injection USP
The Issue: CGMP Deviations: Precautions taken due to Out-of-specification for
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Chloride 0.9% Injection
The Issue: CGMP Deviation: Chemical indicators were not positioned properly
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PrediniSONE Tablets
The Issue: Labeling: Incorrect or Missing Exp Date - An
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PEPPERMINT LIP MOISTURIZER (oxybenzone (4%) and Octinoxate (7%) SPF 15
The Issue: Superpotent drug: This lot of SPF containing lip
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) patches
The Issue: Defective Delivery System: Out of specification for mechanical
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) patches
The Issue: Defective Delivery System: Out of specification for mechanical
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) patches
The Issue: Defective Delivery System: Out of specification for mechanical
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.