Hospira Inc. recalls Lactated Ringer's and 5% Dextrose Injection, USP, 1000 mL flexible containers, Rx only, Hospira, Inc., Lake Forest, IL 6
Recalled April 24, 2013 · FDA recall D-263-2013 · Hospira
Hazard
Non-Sterility: One confirmed customer report that product contained spore-like particulates, consistent with mold. · FDA Class I
Units
136,224 flexible containers
Sold at
Nationwide
Description
Non-Sterility: One confirmed customer report that product contained spore-like particulates, consistent with mold.
Product
Lactated Ringer's and 5% Dextrose Injection, USP, 1000 mL flexible containers, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7929-09.
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →