Hospira Inc. recalls 70% Dextrose Injection USP, 2000 mL, Rx Only, by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7120-07
Recalled July 3, 2013 · FDA recall D-612-2013 · Hospira
Hazard
Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags. · FDA Class II
Units
14,706 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
70% Dextrose Injection USP, 2000 mL, Rx Only, by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7120-07
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →