PlainRecalls
FDA Drug Moderate Class II Terminated

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

Reported: April 27, 2016 Initiated: March 8, 2016 #D-0831-2016

Product Description

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

Reason for Recall

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

Details

Recalling Firm
Hospira Inc.
Units Affected
22292 bags
Distribution
US: Nationwide and Singapore
Location
Lake Forest, IL

Frequently Asked Questions

What product 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. Recalled by Hospira Inc.. Units affected: 22292 bags.
Why was this product recalled?
Chemical Contamination: Potential for contamination of the products with an aromatic hydrocarbon resin.
Which agency issued this recall?
This recall was issued by the FDA Drug on April 27, 2016. Severity: Moderate. Recall number: D-0831-2016.