PlainRecalls
FDA Drug Moderate Class II Terminated

5% Dextrose and 0.45% Sodium Chloride Injection, USP, 1000 mL VisIV Container, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7926-48

Reported: July 3, 2013 Initiated: May 4, 2012 #D-615-2013

Product Description

5% Dextrose and 0.45% Sodium Chloride Injection, USP, 1000 mL VisIV Container, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7926-48

Reason for Recall

Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags.

Details

Recalling Firm
Hospira Inc.
Units Affected
74,256 units
Distribution
Nationwide Puerto Rico, U.S. Virgin Island, Libya, Saudi Arabia
Location
Lake Forest, IL

Frequently Asked Questions

What product was recalled?
5% Dextrose and 0.45% Sodium Chloride Injection, USP, 1000 mL VisIV Container, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7926-48. Recalled by Hospira Inc.. Units affected: 74,256 units.
Why was this product recalled?
Lack of Assurance of Sterility: Hospira, Inc is voluntarily recalling the products due to possible leaking bags.
Which agency issued this recall?
This recall was issued by the FDA Drug on July 3, 2013. Severity: Moderate. Recall number: D-615-2013.