April 2012 FDA Recall Drug by Apotex Corp.
D-1443-2012 - Tablet Thickness

This Class II drug recall was voluntarily initiated by Apotex Corp. on April 5, 2012 for the product Drug. The FDA reported the reason for recall as tablet thickness. The product was distributed Nationwide and the recall is currently terminated.

Recall Number: D-1443-2012

Reason for Recall
Tablet Thickness: Recall was initiated due to the presence of one slightly oversized tablet in a bottle of the identified lot.
Initiated
04-05-2012
Reported
08-15-2012
Quantity
1,749 Bottles

Recall Profile & Regulatory Data

Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Meloxicam Tablets, USP, 15 mg, Rx Only, 100 Tablets per Bottle, Manufactured by: Strides Acrolab Ltd., Bangalore-560 076, India, Manufactured for: Apotex Corp., Weston, FL 33326, NDC 60505-3579-1.

Batch or Lot Expiration Information

Lot# Lot: 7212558, Exp 12/12.