PlainRecalls
FDA Drug Moderate Class II Terminated

0.9% Sodium Chloride Injection, USP, 100mL, VisIV Container, Rx only, Hospira Inc., Lake Forest, IL 60045, NDC 0409-7984-11

Reported: January 14, 2015 Initiated: December 22, 2014 #D-0334-2015

Product Description

0.9% Sodium Chloride Injection, USP, 100mL, VisIV Container, Rx only, Hospira Inc., Lake Forest, IL 60045, NDC 0409-7984-11

Reason for Recall

Lack of Assurance of Sterility: The product has the potential for solution to leak at the administrative port.

Details

Recalling Firm
Hospira Inc.
Units Affected
30840 bags
Distribution
Nationwide
Location
Lake Forest, IL

Frequently Asked Questions

What product was recalled?
0.9% Sodium Chloride Injection, USP, 100mL, VisIV Container, Rx only, Hospira Inc., Lake Forest, IL 60045, NDC 0409-7984-11. Recalled by Hospira Inc.. Units affected: 30840 bags.
Why was this product recalled?
Lack of Assurance of Sterility: The product has the potential for solution to leak at the administrative port.
Which agency issued this recall?
This recall was issued by the FDA Drug on January 14, 2015. Severity: Moderate. Recall number: D-0334-2015.