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, NDC 0338-0049-38.

Reported: July 31, 2019 Initiated: July 18, 2019 #D-1514-2019

Product Description

0.9% Sodium Chloride Injection USP, 100 mL Viaflex Container, Rx Only, Baxter Healthcare Corporation, Deerfield, IL 60015, USA, NDC 0338-0049-38.

Reason for Recall

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

Details

Units Affected
139,680 Containers
Distribution
Nationwide in the United States and Puerto Rico.
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, NDC 0338-0049-38.. Recalled by Baxter Healthcare Corporation. Units affected: 139,680 Containers.
Why was this product recalled?
Lack of Assurance of Sterility: Bags have potential to leak.
Which agency issued this recall?
This recall was issued by the FDA Drug on July 31, 2019. Severity: Moderate. Recall number: D-1514-2019.