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 11621–11640 of 17,529 recalls
Recalled Item: CAP-BIOTIN 100 MG
The Issue: Labeling: Label Mix-Up: Products labeled Biotin 100 mg
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All fluoxymesterone Products
The Issue: Lack of Processing Controls
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All fluconazole Products
The Issue: Lack of Processing Controls
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All hydrocortisone Products
The Issue: Lack of Processing Controls
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All monobenzone Products
The Issue: Lack of Processing Controls
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Simvastatin Tablets
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Escitalopram Tablets USP 20 mg
The Issue: Labeling: Incorrect or Missing Lot and/or Expiration Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zemplar (paricalcitol) capsules
The Issue: Failed Content Uniformity Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Magnesium Sulfate Inj.
The Issue: Presence of Particulate Matter: Confirmed customer complaint for
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Renovo Patch (Capsaicin
The Issue: Marketed Without An Approved NDA/ANDA: product is an
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ORIS (chlorhexidine gluconate)
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Chlorhexidine gluconate
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PerioRx (chlorhexidine gluconate)
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Magnesium Sulfate Inj.
The Issue: Failed pH Specifications: Confirmed high out of specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 8.4% Sodium Bicarbonate Injection
The Issue: Presence of Particulate Matter: particulate matter identified as
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fenofibrate Capsules (Micronized) 134 mg
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: Fenofibrate Capsules (Micronized) 200 mg
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: Ciprofloxacin Ophthalmic Solution (0.3% as base)
The Issue: Failed Quality Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Quelicin (Succinylcholine Chloride) Injection
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: Formula 9 (Papaverine 0.9 mg
The Issue: Lack of Assurance of Sterility: incomplete or missing
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.