FDA recall D-0976-2015

Hospira Inc. · Class I · drug

Product

0.9% Sodium Chloride Injection, USP, 250 mL, Rx only, VisIV Container, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-25.

Reason for recall

Presence of Particulate Matter: Confirmed finding of human hair floating in IV solution.

Distribution

Nationwide.

Key facts

Status: Terminated
Initiation date: 2015-03-05
Report date: 2015-05-13
Termination date: 2016-06-09
Voluntary/Mandated: Voluntary: Firm initiated
Location: Lake Forest, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0976-2015