PlainRecalls
FDA Drug Critical Class I Terminated

Lactated Ringer's and 5% Dextrose Injection, USP, 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA; NDC 0409-7929-09.

Reported: April 24, 2013 Initiated: January 25, 2013 #D-262-2013

Product Description

Lactated Ringer's and 5% Dextrose Injection, USP, 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA; NDC 0409-7929-09.

Reason for Recall

Non-Sterility: Confirmed customer complaint of product contaminated with mold.

Details

Recalling Firm
Hospira Inc.
Units Affected
143,136 flexible containers
Distribution
Nationwide
Location
Lake Forest, IL

Frequently Asked Questions

What product was recalled?
Lactated Ringer's and 5% Dextrose Injection, USP, 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA; NDC 0409-7929-09.. Recalled by Hospira Inc.. Units affected: 143,136 flexible containers.
Why was this product recalled?
Non-Sterility: Confirmed customer complaint of product contaminated with mold.
Which agency issued this recall?
This recall was issued by the FDA Drug on April 24, 2013. Severity: Critical. Recall number: D-262-2013.