Arrow International Inc recalls Single-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Catheter, Catheter, Percutaneous The Arrow Single-

Recalled June 21, 2017 · FDA recall Z-2328-2017 · Arrow International

Hazard

Arrow International is recalling the affected product because the packaging may not be completely sealed, which may compromise sterility. · FDA Class II

Units

27,485 units distributed in U.S., 4,371 units distributed internationally

Sold at

Worldwide Distribution - US (nationwide) and Canada

Description

Arrow International is recalling the affected product because the packaging may not be completely sealed, which may compromise sterility.

Product

Single-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Catheter, Catheter, Percutaneous The Arrow Single-Lumen Catheter permits venous access to the central circulation

Manufacturer(s)

Arrow International Inc

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