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: 04…

Recall date

March 8, 2016

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

D-0831-2016

FDA classification

Class II

Brand / firm

Hospira Inc.

Sold / distributed

US: Nationwide and Singapore

Why it was recalled

Chemical Contamination: Potential for contamination of the products with an aromatic hydrocarbon resin.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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