Arrow International Inc recalls AGB+ Multi Lumen Central Venous Catheterization Kit; Product Codes: CDC-42703-XP1A and CDC-47702-XP1A; Exp. Dates Feb 20

Recalled February 28, 2018 · FDA recall Z-0655-2018 · 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

AGB+ Multi Lumen Central Venous Catheterization Kit; Product Codes: CDC-42703-XP1A and CDC-47702-XP1A; Exp. Dates Feb 2018 - Nov 2018

Manufacturer(s)

Arrow International Inc

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