PlainRecalls
FDA Drug Critical Class I Terminated

0.9% Sodium Chloride Injection, USP, 100 mL flexible container, Rx only, Hospira, Inc. Lake Forest, IL 60045 --- NDC 0409-7984-23

Reported: September 4, 2013 Initiated: August 31, 2012 #D-922-2013

Product Description

0.9% Sodium Chloride Injection, USP, 100 mL flexible container, Rx only, Hospira, Inc. Lake Forest, IL 60045 --- NDC 0409-7984-23

Reason for Recall

Presence of Particulate Matter; product may contain fibrous material

Details

Recalling Firm
Hospira Inc.
Units Affected
264,432 bags
Distribution
Nationwide
Location
Lake Forest, IL

Frequently Asked Questions

What product was recalled?
0.9% Sodium Chloride Injection, USP, 100 mL flexible container, Rx only, Hospira, Inc. Lake Forest, IL 60045 --- NDC 0409-7984-23. Recalled by Hospira Inc.. Units affected: 264,432 bags.
Why was this product recalled?
Presence of Particulate Matter; product may contain fibrous material
Which agency issued this recall?
This recall was issued by the FDA Drug on September 4, 2013. Severity: Critical. Recall number: D-922-2013.