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 13541–13560 of 17,529 recalls
Recalled Item: EDGE Amplified Weight Release capsules
The Issue: Undeclared Phenolphthalein
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: iNDiGO capsules
The Issue: Undeclared Phenolphthalein
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: iNSANE Bee Pollen capsules
The Issue: Undeclared Phenolphthalein
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BtRiM Max capsules
The Issue: Undeclared Phenolphthalein
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AMPD GOLD Bee Pollen capsules
The Issue: Undeclared Sildenafil
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KETOROLAC Tromethamine Inj.
The Issue: Crystallization
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nicardipine Hydrochloride Injection
The Issue: Subpotent Drug and Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KETOROLAC Tromethamine Inj.
The Issue: Crystallization
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketorolac Tromethamine Ophthalmic Solution
The Issue: Presence of Particulate Matter: lot is not meeting
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levetiracetam
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Avastin (Bevacizumab) 1.25 mg/0.05 mL syringe
The Issue: Non-Sterility: Product tested positive for bacterial contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection
The Issue: Presence of Particulate Matter; Hospira has identified the
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Avastin (Bevacizumab) 2 mg/0.08 mL syringe
The Issue: Non-Sterility: Product tested positive for bacterial contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL Citrate
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL Citrate
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system)
The Issue: Defective Delivery System: One lot exceeded the mechanical
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5-methyltetrahydrofolate Calcium (L) (a) 1 gm in 2 oz container
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Benzonatate Capsules
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Practi-0.9% Sodium Chloride
The Issue: Non-sterility: Product is made in a non-sterile facility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Glycopyrrolate injection
The Issue: Labeling: Incorrect or missing Lot and/or Exp Date:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.