drugs Class II Updated 2013-07-03

Hospira Inc. recalls 20% Dextrose Injection, USP, a) 500 mL in 1000 mL Partial-Fi

Recalled Product

20% Dextrose Injection, USP, a) 500 mL in 1000 mL Partial-Fill Container (NDC 0409-7935-19), b) 500 mL VisIV Container (NDC 0409-7953-30), c) 1000 mL VisIV Container, (NDC 0409-7953-48), Rx Only, Hospira, Inc., Lake Forest, IL 60045

Hazard / Issue

Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot #: a) 09-183-JT, Exp 3/13; b) 01-081-JT, Exp 7/12; c) 07-078-JT, 91-083-JT, Exp 7/12
View official government recall

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