FDA recall record

Atorvastatin Calcium Tablets, USP 40 mg*, 1,000 count bottles recall — FDA D-0153-2020

Presence of Foreign Tablets/Capsules: a single tablet of Pravastatin 40 mg found in bottle of Atorvastatin Calcium 40 mg.

Class IIIclassification
D-0153-2020official record ID
Nov 6, 2019report date

Recall record at a glance

Official recordD-0153-2020
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmApotex Inc.
Report dateNov 6, 2019
Recall initiation dateOct 22, 2019
Quantity1968 bottles
LocationNorth York, Canada

Official product description

Atorvastatin Calcium Tablets, USP 40 mg*, 1,000 count bottles, Rx Only, Manufactured by: Apotex Inc. Toronto, Ontario Canada M9L 1T9 Manufactured for: Apotex Corp. Weston, Florida 33326 NDC 60505-2580-8

Why the product was recalled

Presence of Foreign Tablets/Capsules: a single tablet of Pravastatin 40 mg found in bottle of Atorvastatin Calcium 40 mg.

Distribution information

IL, MS, NJ, OH, TX

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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