Arrow International Inc recalls ARROWg+ard Blue Two Lumen Hemodialysis Catheterization Kit for High Volume Infusions; Product Codes: AK-22142-CDC, AK-2…

Recall date

October 17, 2017

Source

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

Recall number

Z-0658-2018

FDA classification

Class II

Brand / firm

Arrow International Inc

Sold / distributed

Distribution US Nationwide

Why it was recalled

These finished good kits may contain the incorrect Springwire Guide (SWG).

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

ARROWg+ard Blue Two Lumen Hemodialysis Catheterization Kit for High Volume Infusions; Product Codes: AK-22142-CDC, AK-22142-F, AK-25142-CDC, AK-25142-F; Exp. Dates Feb 2018 - Nov 2018