GLIMEPIRIDE TABLETS USP, 2 mg, 100-count tablets per bottle, Rx only, Manufactured for: Qualitest Pharmaceuticals, Huntsville, AL 35811, NDC 0603-3745-21.
Reported: May 1, 2013 Initiated: April 19, 2013 #D-298-2013
Product Description
GLIMEPIRIDE TABLETS USP, 2 mg, 100-count tablets per bottle, Rx only, Manufactured for: Qualitest Pharmaceuticals, Huntsville, AL 35811, NDC 0603-3745-21.
Reason for Recall
Failed Tablet/Capsule Specifications: One oversized tablet was found in a sealed 100 count bottle of Glimepiride at the retail level.
Details
- Recalling Firm
- Qualitest Pharmaceuticals
- Units Affected
- 10,373 bottles
- Distribution
- Nationwide
- Location
- Huntsville, AL
Frequently Asked Questions
What product was recalled? ▼
GLIMEPIRIDE TABLETS USP, 2 mg, 100-count tablets per bottle, Rx only, Manufactured for: Qualitest Pharmaceuticals, Huntsville, AL 35811, NDC 0603-3745-21.. Recalled by Qualitest Pharmaceuticals. Units affected: 10,373 bottles.
Why was this product recalled? ▼
Failed Tablet/Capsule Specifications: One oversized tablet was found in a sealed 100 count bottle of Glimepiride at the retail level.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on May 1, 2013. Severity: Moderate. Recall number: D-298-2013.
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