Hospira Inc. recalls Lactated Ringer's and 5% Dextrose Injection, USP, 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60
Recalled April 24, 2013 · FDA recall D-262-2013 · Hospira
Hazard
Non-Sterility: Confirmed customer complaint of product contaminated with mold. · FDA Class I
Units
143,136 flexible containers
Sold at
Nationwide
Description
Non-Sterility: Confirmed customer complaint of product contaminated with mold.
Product
Lactated Ringer's and 5% Dextrose Injection, USP, 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA; NDC 0409-7929-09.
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →