FDA recall record

Apotex Meloxicam Tablets, USP, 15 mg recall — FDA D-1443-2012

Tablet Thickness: Recall was initiated due to the presence of one slightly oversized tablet in a bottle of the identified lot.

Class IIclassification
D-1443-2012official record ID
Aug 15, 2012report date

Recall record at a glance

Official recordD-1443-2012
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmApotex Corp.
Report dateAug 15, 2012
Recall initiation dateApr 5, 2012
Quantity1,749 Bottles
LocationWeston, FL, United States

Official 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.

Why the product was recalled

Tablet Thickness: Recall was initiated due to the presence of one slightly oversized tablet in a bottle of the identified lot.

Distribution information

Nationwide

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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