FDA recall record

Apotex Piperacillin and Tazobactam for Injection, USP 4.5 gram/vial* 10-count Single Use recall — FDA D-0840-2018

Subpotent Drug: High Levels of Impurities Resulting in Decrease Potency

Class Iclassification
D-0840-2018official record ID
May 23, 2018report date

Recall record at a glance

Official recordD-0840-2018
CategoryDrug Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmApotex Inc.
Report dateMay 23, 2018
Recall initiation dateMay 8, 2018
Quantity13453 vials
LocationNorth York, Canada

Official product description

Piperacillin and Tazobactam for Injection, USP 4.5 gram/vial* 10-count Single Use Vials per carton, Rx only, Mfg. by: Hospira Healthcare India Pvt. Ltd. Irungattukottai-602 105, India Mfg. for: Apotex Corp. Weston, FL 33326. NDC 60505-0688-4

Why the product was recalled

Subpotent Drug: High Levels of Impurities Resulting in Decrease Potency

Distribution information

Nationwide in the USA.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly 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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