D-1443-2012 Class II Terminated
FDA drug recall D-1443-2012 was initiated by Apotex Corp. on Apr 5, 2012 and is designated Class II. Reason for recall: Tablet Thickness: Recall was initiated due to the presence of one slightly oversized tablet in a bottle of the identified lot. The recall status is terminated (terminated Sep 19, 2013). Affected quantity: 1,749 Bottles.
Recall Details
- Product Type
- Drugs
- Report Date
- Aug 15, 2012
- Initiation Date
- Apr 5, 2012
- Termination Date
- Sep 19, 2013
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1,749 Bottles
Product Description
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.
Reason for Recall
Tablet Thickness: Recall was initiated due to the presence of one slightly oversized tablet in a bottle of the identified lot.
Distribution Pattern
Nationwide
Code Information
Lot: 7212558, Exp 12/12.
Source
- Dataset
- openFDA drug recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for D-1443-2012
- openFDA file date
- Oct 26, 2026
- Loaded by RegDataLab
- Oct 27, 2026