Hospira Inc. recalls 5% Dextrose and 0.45% Sodium Chloride Injection, USP, 1000 mL VisIV Container, Hospira, Inc., Lake Forest, IL 60045, NDC
Recalled July 3, 2013 · FDA recall D-615-2013 · Hospira
Hazard
Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags. · FDA Class II
Units
74,256 units
Sold at
Nationwide Puerto Rico, U.S. Virgin Island, Libya, Saudi Arabia
Description
Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags.
Product
5% Dextrose and 0.45% Sodium Chloride Injection, USP, 1000 mL VisIV Container, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7926-48
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →