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.

FDA recall notice · announced April 24, 2013 · Hospira

Class I FDA/FSIS Class I: reasonable probability that use will cause serious adverse health consequences or death.

The product

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.

Notes

Distribution: Nationwide
Lot/code information: Lot #: 05-019-JT*, Exp 05/01/13; lot number * may be followed by 01, 90, or 91.
Quantity: 143,136 flexible containers
Status: Terminated
Products in this recall event:
- 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. (D-262-2013)

Source: U.S. Food and Drug Administration public recall data. This page reports official records and is not legal, medical, or repair advice.