PlainRecalls
FDA Drug Critical Class I Terminated

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

Reported: May 13, 2015 Initiated: March 5, 2015 #D-0976-2015

Product Description

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.

Details

Recalling Firm
Hospira Inc.
Units Affected
9,912 VisIV flex containers
Distribution
Nationwide.
Location
Lake Forest, IL

Frequently Asked Questions

What product was recalled?
0.9% Sodium Chloride Injection, USP, 250 mL, Rx only, VisIV Container, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-25.. Recalled by Hospira Inc.. Units affected: 9,912 VisIV flex containers.
Why was this product recalled?
Presence of Particulate Matter: Confirmed finding of human hair floating in IV solution.
Which agency issued this recall?
This recall was issued by the FDA Drug on May 13, 2015. Severity: Critical. Recall number: D-0976-2015.