Home / Recalls / AmeriSource Bergen / D-1066-2013

D-1066-2013 Class II Terminated

Recalled by AmeriSource Bergen — Chesterbrook, PA

Recall Details

Product Type: Drugs
Report Date: October 9, 2013
Initiation Date: September 13, 2013
Termination Date: October 1, 2014
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 60 vials

Product Description

Ifosfamide Injection 3g/60 mL, 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 0069-4496-22

Reason for Recall

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

Distribution Pattern

Nationwide

Code Information

Lot #s: 7800929, 7800931, Exp 02/15; 7800962, Exp 03/15