FDA recall D-836-2013

Hospira Inc. · Class I · drug

Product

0.9% Sodium Chloride Injection, USP, 1000 mL flexible container, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-09.

Reason for recall

Presence of Particulate Matter: reports of small grey/brown particles found in the primary container identified as brass particulates

Distribution

Nationwide

Key facts

Status
Terminated
Initiation date
2013-03-29
Report date
2013-08-14
Termination date
2015-07-20
Voluntary/Mandated
Voluntary: Firm initiated
Location
Lake Forest, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-836-2013