drugs Class II Updated 2013-03-13

Hospira Inc. recalls HEXTEND 6% Hetastarch in Lactated Electrolyte Injection, 500

Recalled Product

HEXTEND 6% Hetastarch in Lactated Electrolyte Injection, 500 mL, Rx only , MANUFACTURED AND DISTRIBUTED BY HOSPIRA, INC., LAKE FOREST, IL 60045, NDC 0409-1555-54

Hazard / Issue

Lack of Assurance of Sterility: There is the potential for the solution to leak from the seal of the fill tube to the bag.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot # 10-199-JT Exp. 10/13
View official government recall

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