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 5301–5320 of 17,529 recalls
Recalled Item: Diethylpropion
The Issue: cMGP Deviations: Drug products repackaged into pouches without
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Phentermine
The Issue: cMGP Deviations: Drug products repackaged into pouches without
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diethylpropion
The Issue: cMGP Deviations: Drug products repackaged into pouches without
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nymalize (nimodipine) oral solution
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Albuterol Sulfate Inhalation Aerosol
The Issue: Defective Delivery System: Sustained trend of failure to
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Genesis Hand Sanitizer Gel
The Issue: CGMP Deviations: hand sanitizers were recalled because they
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Panagel Hand Sanitizer
The Issue: CGMP Deviations: hand sanitizers were recalled because they
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Genesis Hand Sanitizer Gel
The Issue: CGMP Deviations: hand sanitizers were recalled because they
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Killz Germz Hand Sanitizer
The Issue: Sub-Potent Drug; Killz GERMz was recalled due to
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Killz Germz Hand Sanitizer
The Issue: Sub-Potent Drug; Killz GERMz was recalled due to
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: M Hand Sanitizer Ethyl Alcohol Antiseptic 80%v/v
The Issue: Chemical Contamination and Subpotent Drug: FDA analysis found
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Citalopram Oral Solution
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nicotine Gum
The Issue: Labeling: Incorrect or Missing Package Insert: The package
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Buprenorphine Transdermal System 5 mcg/hour
The Issue: Failed Stability Specifications: Below specification result for buprenorphine
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eye Itch Relief
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: bio aaa Alcohol en Gel Antibacterial
The Issue: CGMP Deviations: Product manufactured in a facility where
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Leafree Instant Hand Sanitizer Aloe Vera (ethyl alcohol 70% v/v)
The Issue: Marketed without an Approved NDA/ANDA; product labeled as
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HAND SANITIZER (alcohol 80%)
The Issue: CGMP Deviations: Product contains acetaldehyde and acetal above
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HAND SANITIZER (alcohol 80%)
The Issue: CGMP Deviations: Product manufactured in same facility where
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: pH-D Feminine Health Boric Acid Vaginal Suppositories
The Issue: Marketed without an Approved NDA/ANDA
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.