Arrow QuickFlash Catheterization Kit Recall Issued Following Reports of Life-Threatening Blood Vessel Damage
At least 10 patient injuries and one death have been reported in connection to the Arrow QuickFlash catherization kit recall.
At least 10 patient injuries and one death have been reported in connection to the Arrow QuickFlash catherization kit recall.
The manufacturer has received at least 83 complaints of the recalled Arrow Catheter Systems separating while inside a patient’s vein, resulting in more than a dozen injuries.
Manufacturer warns the aortic balloon pump may fail prematurely due to rapid battery depletion, leading to a disruption in treatment.
Reports of the filters splitting and detaching have led to dozens of complaints and at least four injury reports