Arrow International Inc recalls Pressure Injectable ARROWg+ard Blue PLUS Multi Lumen Central Venous Catheterization Kit; Product Code: ASK 42703 PUHC; E

Recalled February 28, 2018 · FDA recall Z-0647-2018 · 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

Pressure Injectable ARROWg+ard Blue PLUS Multi Lumen Central Venous Catheterization Kit; Product Code: ASK 42703 PUHC; Exp. Dates Feb 2018 - Nov 2018

Manufacturer(s)

Arrow International Inc

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