Arrow International Inc recalls Arterial Catheterization Kit, Arterial Line Kit with Sharps Safety Features wire, guide, catheter The Arrow Arterial

Recalled June 21, 2017 · FDA recall Z-2327-2017 · 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 distributed in the U.S, 4,371 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

Arterial Catheterization Kit, Arterial Line Kit with Sharps Safety Features wire, guide, catheter The Arrow Arterial Catheterization device permits access to the peripheral arterial circulation or to other small vessels

Manufacturer(s)

Arrow International Inc

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