FDAFDA · Food and drugs·Recall number D-1066-2013
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
Published October 9, 2013 · Recall initiated: September 13, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Temperature abuse: Certain vials of Ifosfamide IV products were not refrigerated at certain Amerisource Bergen Drug Corp distribution centers.
What to do
Voluntary: Firm initiated · Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Recall details
- Manufacturer
- AmeriSource Bergen
- Distributor
- Nationwide
- Lot
- Lot #s: 7800929, 7800931, Exp 02/15; 7800962, Exp 03/15
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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