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Arrow International Inc recalls Pressure Injectable Arrowg+ard Blue Plus Multi-Lumen Central Venous Catheterization Kit. Permits venous access to centr
Recalled May 3, 2017 · FDA recall Z-1879-2017 · Arrow International
Hazard
Arrow International is recalling due to possible voids in the catheter hub, which could lead to an interlumen crossover. · FDA Class II
Units
310 units
Sold at
US Distribution to NJ, IL, and PA
Description
Arrow International is recalling due to possible voids in the catheter hub, which could lead to an interlumen crossover.
Product
Pressure Injectable Arrowg+ard Blue Plus Multi-Lumen Central Venous Catheterization Kit. Permits venous access to central circulation by way of subclavian, jugular and femoral veins. The ARROWg+ard technology is intended to provide protection against catheter-related bloodstream infections (CRBSIs). It is not intended to be used as a treatment for existing infections nor is it indicated for long-term use (>30 days). Clinical effectiveness of the ARROW g+ard Blue Plus catheter in preventing CRBSIs compared to the original ARROWg+ard Blue catheter has not been studied
Manufacturer(s)
Arrow International Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →