FDAFDA · Food and drugs·Recall number D-298-2013
GLIMEPIRIDE TABLETS USP, 2 mg, 100-count tablets per bottle, Rx only, Manufactured for: Qualitest Pharmaceuticals, Huntsville, AL 35811, NDC 0603-3745-21.
Published May 1, 2013 · Recall initiated: April 19, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed Tablet/Capsule Specifications: One oversized tablet was found in a sealed 100 count bottle of Glimepiride at the retail level.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Qualitest Pharmaceuticals
- Distributor
- Nationwide
- Lot
- Lot #: C0671212A, Exp 12/14
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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