Arrow International Inc recalls ARROWg+ard Blue Two Lumen Hemodialysis Catheterization Kit for High Volume Infusions; Product Codes: AK-22142-CDC, AK-22

Recalled February 28, 2018 · FDA recall Z-0658-2018 · Arrow International

Hazard

These finished good kits may contain the incorrect Springwire Guide (SWG). · FDA Class II

Units

5,926 total

Sold at

Distribution US Nationwide

Description

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

Product

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

Manufacturer(s)

Arrow International Inc

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →