PlainRecalls
FDA Drug Moderate Class II Terminated

0.9% Sodium Chloride Injection, USP, 100 mL VIAFLEX Container, Rx Only, Baxter Healthcare Corporation, Deerfield IL 60015 USA, Product Code: 2B1309, NDC: 0338-0049-38

Reported: July 19, 2017 Initiated: July 6, 2017 #D-0973-2017

Product Description

0.9% Sodium Chloride Injection, USP, 100 mL VIAFLEX Container, Rx Only, Baxter Healthcare Corporation, Deerfield IL 60015 USA, Product Code: 2B1309, NDC: 0338-0049-38

Reason for Recall

Lack of Assurance of Sterility: Bags have the potential to leak.

Details

Units Affected
295,200 bags
Distribution
Nationwide, Puerto Rico and Saudi Arabia
Location
Deerfield, IL

Frequently Asked Questions

What product was recalled?
0.9% Sodium Chloride Injection, USP, 100 mL VIAFLEX Container, Rx Only, Baxter Healthcare Corporation, Deerfield IL 60015 USA, Product Code: 2B1309, NDC: 0338-0049-38. Recalled by Baxter Healthcare Corporation. Units affected: 295,200 bags.
Why was this product recalled?
Lack of Assurance of Sterility: Bags have the potential to leak.
Which agency issued this recall?
This recall was issued by the FDA Drug on July 19, 2017. Severity: Moderate. Recall number: D-0973-2017.