PlainRecalls
FDA Drug Critical Class I Terminated

0.9% Sodium Chloride Injection USP, 50 mL Single Dose VIAFLEX Container bags, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015, Product Code 2B1301, NDC 0338-0049-11.

Reported: August 26, 2015 Initiated: July 17, 2015 #D-1336-2015

Product Description

0.9% Sodium Chloride Injection USP, 50 mL Single Dose VIAFLEX Container bags, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015, Product Code 2B1301, NDC 0338-0049-11.

Reason for Recall

Presence of Particulate Matter: Customer complaint for an insect found free floating inside a single bag for each lot recalled.

Details

Recalling Firm
Baxter Healthcare Corp.
Units Affected
189,120 bags
Distribution
Nationwide
Location
Deerfield, IL

Frequently Asked Questions

What product was recalled?
0.9% Sodium Chloride Injection USP, 50 mL Single Dose VIAFLEX Container bags, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015, Product Code 2B1301, NDC 0338-0049-11.. Recalled by Baxter Healthcare Corp.. Units affected: 189,120 bags.
Why was this product recalled?
Presence of Particulate Matter: Customer complaint for an insect found free floating inside a single bag for each lot recalled.
Which agency issued this recall?
This recall was issued by the FDA Drug on August 26, 2015. Severity: Critical. Recall number: D-1336-2015.