Drug recall
Meloxicam Tablets, USP, 15 mg, Rx Only, 100 Tablets per Bottle, Manufactured by: Strides Acrolab Ltd…
FDA recall event 62436 · Class II · Apotex Corp.
Key facts
| Event ID | 62436 |
|---|---|
| Recall numbers | D-1443-2012 |
| Recalling firm | Apotex Corp. |
| Product type | Drugs |
| Products | 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. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Tablet Thickness: Recall was initiated due to the presence of one slightly oversized tablet in a bottle of the identified lot. |
| Initiation date | Apr 5, 2012 |
| Report date | Aug 15, 2012 |
| Termination date | Sep 19, 2013 |
| City | Weston |
| State | FL |
| Country | United States |
| FEI number | 3006727872 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: