RecallDepth
Class II Terminated

Ifosfamide Injection 1g/20mL, Single dose vial, Rx only, Sterile, For Intravenous Use, Refrigerate at 2-8 degrees celcius, Distributed by Pfizer Labs, Division of Pfizer Inc., New York, NY 10017, NDC 0069-4495-22

This recall has been terminated (originally issued October 9, 2013).

Company
Amerisource Bergen
Recall Initiated
September 13, 2013
Posted
October 9, 2013
Recall Number
D-1065-2013
Voluntary / Mandated
Voluntary: Firm initiated
Quantity
49 vials
Firm Location
Chesterbrook, PA, United States
Official Source
View on FDA website ↗

Reason for Recall

Temperature abuse: Certain vials of Ifosfamide IV products were not refrigerated at certain Amerisource Bergen Drug Corp distribution centers.

Distribution

Nationwide

Lot / Code Info

Lot #s: 7800932, 7800933, exp 02/15

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