FDA recall D-262-2013

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.

Distribution

Nationwide

Key facts

Status

Terminated

Initiation date

2013-01-25

Report date

2013-04-24

Termination date

2015-08-21

Voluntary/Mandated

Voluntary: Firm initiated

Location

Lake Forest, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-262-2013