FDA recall record

Apotex Candesartan Cilexetil Tablets, 8 mg, 30-count bottle recall — FDA D-0242-2015

Failed Impurities/Degradation Specifications: Out of specification (OOS) results were observed for CAD-II, CAD-V and Total Impurities.

Class IIIclassification
D-0242-2015official record ID
Nov 12, 2014report date

Recall record at a glance

Official recordD-0242-2015
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmApotex Inc.
Report dateNov 12, 2014
Recall initiation dateOct 16, 2014
Quantity18,493
LocationToronto, N/A, Canada

Official product description

Candesartan Cilexetil Tablets, 8 mg, 30-count bottle, Rx Only, Manufactured by Apotex Research Pvt. Ltd., Bangalore- 560 099, India, Manufactured for Apotex Corp., Weston, FL 33326, NDC 60505-3619-3

Why the product was recalled

Failed Impurities/Degradation Specifications: Out of specification (OOS) results were observed for CAD-II, CAD-V and Total Impurities.

Distribution information

Nationwide.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement 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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