Hospira Inc. recalls Dextrose Injection, USP, 50%, Packaged as 500 mL in 1000 mL Bag, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 040
Recalled April 27, 2016 · FDA recall D-0828-2016 · Hospira
Hazard
Chemical Contamination: Potential for contamination of the products with an aromatic hydrocarbon resin. · FDA Class II
Units
4368 bags
Sold at
US: Nationwide and Singapore
Description
Chemical Contamination: Potential for contamination of the products with an aromatic hydrocarbon resin.
Product
Dextrose Injection, USP, 50%, Packaged as 500 mL in 1000 mL Bag, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7936-19, Barcode (01) 0 030409 793619 9
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →