Recall: Ifosfamide Injection 1g/20mL, Single dose vial, Rx only, Sterile IV Use

Product Detail

Product Description 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

Recall Number D-1065-2013

Classification Class II

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

Product Distributed Qty 49 vials

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

Event Detail

Event Id 66316

Product Type Drugs

Status Ongoing

Recalling Firm

AmeriSource Bergen

City Chesterbrook
State PA
Country US

Voluntary / Mandated Voluntary: Firm Initiated

Recall Initiation Date 2013-09-13

Initial Firm Notification of Consignee or Public Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Distribution Pattern Nationwide