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 11101–11120 of 17,529 recalls
Recalled Item: Carvediol Tablets
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carvediol Tablets
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carvediol Tablets
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amoxicillin for Oral Suspension USP
The Issue: Superpotent drug: Out of specification test result for
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diazepam Injection USP 10mg/2mL (5 mg/mL
The Issue: Crystallization: Product contains particulate identified to be crystallized
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Albuterol Sulfate Syrup
The Issue: Presence of Foreign Substance; presence of black particles
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alprazolam Extended-release Tablets
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Papaverine 30 mg / Phentolamine 1 mg / mL -- 5 mL GLASS VIAL
The Issue: Lack of assurance of sterility: This recall includes
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Calcium Gluconate 1% -- 1000 mL VIAFLEX IV BAG
The Issue: Lack of assurance of sterility: This recall includes
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Calcium Gluconate 2.5% -- 20 mL PLASTIC SYRINGE
The Issue: Lack of assurance of sterility: This recall includes
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Papaverine 75 mg / Phentolamine 2.5 mg / Prostaglandin 25
The Issue: Lack of assurance of sterility: This recall includes
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prostaglandin 200 mcg/ 0.1 mL -- 25 mL GLASS VIAL
The Issue: Lack of assurance of sterility: This recall includes
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eptifibatide Injection 75 mg/100 mL (0.75 mg/mL) single use vial
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Linezolid Injection 600 mg/300 mL Rx Only
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ondansetron Injection USP 40 mg/20 mL (2 mg/mL)
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ARGATROBAN Injection in 0.9% Sodium Chloride 250 mg/250 mL (1 mg/mL)
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methylprednisolone Tablets
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxacillin for Injection
The Issue: Presence of Particulate Matter; The firm received two
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SECONAL SODIUM (secobarbital sodium) Capsules
The Issue: Labeling: Incorrect or Missing Package Insert: Package insert
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cyproheptadine Hydrochloride Syrup
The Issue: Subpotency: product assayed and found OOS for cyproheptadine
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.