FDA recall D-1066-2013

AmeriSource Bergen · Class II · drug

Product

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

Nationwide

Key facts

Status
Terminated
Initiation date
2013-09-13
Report date
2013-10-09
Termination date
2014-10-01
Voluntary/Mandated
Voluntary: Firm initiated
Location
Chesterbrook, PA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1066-2013