Arrow International Inc recalls 1) ARROWg+ard Blue You-Blend Two-Lumen Hemodialysis Catheterization Kit for High Volume Infusions The large-bore two-lu

Recalled June 21, 2017 · FDA recall Z-2334-2017 · 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 the 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

1) ARROWg+ard Blue You-Blend Two-Lumen Hemodialysis Catheterization Kit for High Volume Infusions The large-bore two-lumen catheter permits venous access to the central circulation for rapid fluid administration, temporary or acute hemodialysis, apheresis and hemofiltration. It may be inserted into the jugular, subclavia, or femoral veins Catheter, hemodialysis non-implanted

Manufacturer(s)

Arrow International Inc

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