Baxter Healthcare Corp. recalls 0.9% Sodium Chloride Injection USP MINI-BAG Plus Container, 100 mL VIAFLEX Single Dose Container bags, Rx only, Baxter…

Recall date

July 17, 2015

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

D-1335-2015

FDA classification

Class I

Brand / firm

Baxter Healthcare Corp.

Sold / distributed

Nationwide

Why it was recalled

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

Class I is the FDA’s most serious recall level: there is a reasonable probability that using this product will cause serious harm or death.

What was recalled

0.9% Sodium Chloride Injection USP MINI-BAG Plus Container, 100 mL VIAFLEX Single Dose Container bags, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015, Product Code 2B0043, NDC 0338-0553-18.