RecallDepth
Class III Terminated

TORISEL Kit (temsirolimus) injection, 25 mg/mL, 1 vial of TORISEL 25 mg/mL and 1 vial of 2.2 mL DILUENT per carton, Rx only, Distributed by Wyeth Pharmaceuticals Inc., A subsidiary of Pfizer Inc., Philadelphia, PA 19101; Diluent  MADE IN ITALY; NDC 0008-1179-01.

Company
Pfizer Inc.
Recall Initiated
October 10, 2014
Posted
November 12, 2014
Recall Number
D-0235-2015
Voluntary / Mandated
Voluntary: Firm initiated
Quantity
16,000 kits
Firm Location
New York, NY, United States

Reason for Recall

Crystallization: Impurities in a raw material used to manufacture the diluent can cause the formation of crystals in the diluent vials after cold storage. The TORISEL vials are not affected by this issue.

Distribution

Nationwide and Puerto Rico

Lot / Code Info

Kit Lot #: AIEM/13, Exp 05/16 that contain diluent lots AHZW/11 and AHZW/12

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