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 10121–10140 of 17,529 recalls
Recalled Item: Paliperidone Extended-Release Tablets
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BuPROPion HCL Tablets
The Issue: Failed Moisture Limits: Product tested out-of-specification for moisture
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methocarbamol
The Issue: CGMP Deviations: Lack of quality assurance at the
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CaverFlo Natural Herbal Coffee
The Issue: Undeclared Milk
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BRILINTA (ticagrelor) tablets
The Issue: Presence of Foriegn Tablets/Capsules: customer complaint that an
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mefenamic Acid Capsules
The Issue: Presence of foreign substance: The recall was initiated
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PONSTEL (Mefanamic Acid) USP
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mefenamic Acid
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Caffeine Powder
The Issue: Marketed without an Approved NDA/ANDA: The product consists
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zenatane (isotretinoin) Capsules
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zenatane (isotretinoin) Capsules
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zenatane (isotretinoin) Capsules
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zenatane (isotretinoin) Capsules
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Biotech Underground Tri-Ton Hardcore Formula capsules
The Issue: Marketed Without An Approved NDA/ANDA: Tainted Product Marketed
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fludeoxyglucose F 18 Injection
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levophed norepinephrine bitartrate
The Issue: GMP Deviation; A foreign stopper was observed during
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ceFAZolin sodium added to 100 mL 0.9% Sodium Chloride injectable
The Issue: Lack of assurance of sterility: Product bags leaking
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYDROmorphone HCL in 0.9% Sodium Chloride injectable
The Issue: Lack of assurance of sterility: Product bags leaking
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: morphine sulfate in 0.9% Sodium Chloride injectable
The Issue: Lack of assurance of sterility: Product bags leaking
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL (as citrate) in 0.9% Sodium Chloride injectable
The Issue: Lack of assurance of sterility: Product bags leaking
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.