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

Reason for recall

Non-Sterility: One confirmed customer report that product contained spore-like particulates, consistent with mold.

Notes

Distribution: Nationwide
Lot/code information: Lot # :12-160-JT*, Exp 12/01/13; lot number * may be followed by 01 or 90
Quantity: 136,224 flexible containers
Status: Terminated
Products in this recall event:
- Lactated Ringer's and 5% Dextrose Injection, USP, 1000 mL flexible containers, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7929-09. (D-263-2013)

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