PlainRecalls
FDA Drug Moderate Class II Terminated

5% Dextrose Injection USP, a) 250 mL (NDC 0409-7922-02), b) 500 mL (NDC 0409-7922-30), by Hospira, Inc., Lake Forest, IL 60045

Reported: July 3, 2013 Initiated: May 4, 2012 #D-614-2013

Product Description

5% Dextrose Injection USP, a) 250 mL (NDC 0409-7922-02), b) 500 mL (NDC 0409-7922-30), by Hospira, Inc., Lake Forest, IL 60045

Reason for Recall

Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags.

Details

Recalling Firm
Hospira Inc.
Units Affected
267,288 units
Distribution
Nationwide Puerto Rico, U.S. Virgin Island, Libya, Saudi Arabia
Location
Lake Forest, IL

Frequently Asked Questions

What product was recalled?
5% Dextrose Injection USP, a) 250 mL (NDC 0409-7922-02), b) 500 mL (NDC 0409-7922-30), by Hospira, Inc., Lake Forest, IL 60045. Recalled by Hospira Inc.. Units affected: 267,288 units.
Why was this product recalled?
Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags.
Which agency issued this recall?
This recall was issued by the FDA Drug on July 3, 2013. Severity: Moderate. Recall number: D-614-2013.