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Arrow Teleflex Recalls 847 Chronic Hemodialysis Catheters

ANSM was notified that Arrow International Inc / Teleflex has initiated a product withdrawal (recall action registered as R2610908) affecting chronic hemodialysis catheters. The recall encompasses 847 units across seven product lines including Arrow Edge, Arrow-Clark VectorFlow, Cannon II Plus, and NextStep catheters in both antegrade and retrograde configurations. Healthcare facilities and nephrologists using these devices have been contacted directly via letter from the manufacturer.