PlainRecalls
FDA Drug Moderate Class II Terminated

0.9% Sodium Chloride Injection USP, 500 mL in VIAFLEX Plastic Container, Baxter Healthcare Corporation Deerfield, IL 60015, NDC 0338-0049-03.

Reported: August 19, 2015 Initiated: July 2, 2015 #D-1326-2015

Product Description

0.9% Sodium Chloride Injection USP, 500 mL in VIAFLEX Plastic Container, Baxter Healthcare Corporation Deerfield, IL 60015, NDC 0338-0049-03.

Reason for Recall

Presence of Particulate Matter and Lack of Assurance of Sterility: The firm received a complaint for customer of presence of particulate matter, leaky containers, and missing port protectors.

Details

Recalling Firm
Baxter Healthcare Corp.
Units Affected
189,912 containers
Distribution
TX and TN
Location
Deerfield, IL

Frequently Asked Questions

What product was recalled?
0.9% Sodium Chloride Injection USP, 500 mL in VIAFLEX Plastic Container, Baxter Healthcare Corporation Deerfield, IL 60015, NDC 0338-0049-03.. Recalled by Baxter Healthcare Corp.. Units affected: 189,912 containers.
Why was this product recalled?
Presence of Particulate Matter and Lack of Assurance of Sterility: The firm received a complaint for customer of presence of particulate matter, leaky containers, and missing port protectors.
Which agency issued this recall?
This recall was issued by the FDA Drug on August 19, 2015. Severity: Moderate. Recall number: D-1326-2015.