PlainRecalls
FDA Drug Critical Class I Terminated

0.9% Sodium Chloride Injection, USP, 250 mL, Rx Only, Hospira Inc., Lake Forest, IL, 60045, USA, NDC 0409-7983-02

Reported: April 29, 2015 Initiated: January 20, 2015 #D-0969-2015

Product Description

0.9% Sodium Chloride Injection, USP, 250 mL, Rx Only, Hospira Inc., Lake Forest, IL, 60045, USA, NDC 0409-7983-02

Reason for Recall

Presence of Particulate Matter; Hospira has identified the particulate as a human hair, sealed in the bag at the additive port area.

Details

Recalling Firm
Hospira Inc.
Units Affected
661,128 containers
Distribution
Nationwide
Location
Lake Forest, IL

Frequently Asked Questions

What product was recalled?
0.9% Sodium Chloride Injection, USP, 250 mL, Rx Only, Hospira Inc., Lake Forest, IL, 60045, USA, NDC 0409-7983-02. Recalled by Hospira Inc.. Units affected: 661,128 containers.
Why was this product recalled?
Presence of Particulate Matter; Hospira has identified the particulate as a human hair, sealed in the bag at the additive port area.
Which agency issued this recall?
This recall was issued by the FDA Drug on April 29, 2015. Severity: Critical. Recall number: D-0969-2015.