Hospira Inc. recalls Mannitol I.V., 20%, USP (20 g/ 100 mL), Packaged in 250 mL Bags, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC: 0
Recalled April 27, 2016 · FDA recall D-0831-2016 · Hospira
Hazard
Chemical Contamination: Potential for contamination of the products with an aromatic hydrocarbon resin. · FDA Class II
Units
22292 bags
Sold at
US: Nationwide and Singapore
Description
Chemical Contamination: Potential for contamination of the products with an aromatic hydrocarbon resin.
Product
Mannitol I.V., 20%, USP (20 g/ 100 mL), Packaged in 250 mL Bags, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC: 0409-7715-02, Barcode (01) 0 030409 771502 2
Manufacturer(s)
Hospira Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →