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 5021–5040 of 17,529 recalls
Recalled Item: 0.9% SODIUM CHLORIDE Irrigation
The Issue: Presence of particulate matter.one confirmed customer report of
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gabapentin Oral Solution
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Romidepsin Injecton
The Issue: Failed Impurity/Degradation Specifications: Out-of-specifications results observ
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acetaminophen
The Issue: Labeling: Label Mix-up; The bottle of over-the-counter Acetaminophen
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nortriptyline HCL capsules
The Issue: cGMP deviations: The quantity of active ingredient used
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Menopur 75 IU
The Issue: Failed pH specifications: Out of Specification pH results
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Buprenorphine and Naloxone Sublingual Film 2mg/0.5mg
The Issue: Subpotent drug: Out of specification for assay of
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Progesterone Capsules
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cequa (cyclosporine ophthalmic solution) 0.09%
The Issue: Subpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methylprednisolone Tablets USP
The Issue: Labeling: Illegible label: Customer complaint received of mis-alignment
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atorvastatin Calcium Tablets
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 30 mg over 9 hours
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)
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)
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) Delivers 20 mg over 9 hours
The Issue: Defective Delivery System: Out of specification for mechanical
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acyclovir Sodium Injection 1000mg/20mL (50mg/mL) vial NDC 68382-049-01
The Issue: Crystallization: customer complaints for crystallization in finished product
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acyclovir Sodium Injection 500mg/10mL (50mg/mL) vial NDC 68382-048-01
The Issue: Crystallization: customer complaints for crystallization in finished product
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methacholine Challenge 5-Syringe Test Kits
The Issue: Temperature Abuse; labeled with the incorrect room temperature
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Imatinib Mesylate Tablets 100mg
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fludeoxyglucose F 18 Injection
The Issue: Sterility Concerns
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.