PlainRecalls
FDA Drug Moderate Class II Terminated

0.9% Sodium Chloride Injection, USP, 50 mL, VIAFLEX Plastic Container Multi Pack, Rx Only, Baxter Healthcare Corporation, Deerfield, IL , Product code 2B1308, NDC 0338-0049-31

Reported: April 8, 2015 Initiated: March 23, 2015 #D-0429-2015

Product Description

0.9% Sodium Chloride Injection, USP, 50 mL, VIAFLEX Plastic Container Multi Pack, Rx Only, Baxter Healthcare Corporation, Deerfield, IL , Product code 2B1308, NDC 0338-0049-31

Reason for Recall

Lack of Assurance of Sterility; increased complaints received for leaks

Details

Recalling Firm
Baxter Healthcare Corp
Units Affected
196,128 containers
Distribution
Nationwide and Singapore
Location
Deerfield, IL

Frequently Asked Questions

What product was recalled?
0.9% Sodium Chloride Injection, USP, 50 mL, VIAFLEX Plastic Container Multi Pack, Rx Only, Baxter Healthcare Corporation, Deerfield, IL , Product code 2B1308, NDC 0338-0049-31. Recalled by Baxter Healthcare Corp. Units affected: 196,128 containers.
Why was this product recalled?
Lack of Assurance of Sterility; increased complaints received for leaks
Which agency issued this recall?
This recall was issued by the FDA Drug on April 8, 2015. Severity: Moderate. Recall number: D-0429-2015.