There is the potential for inadequate connection between the top and bottom housings of the Micro Clave Clear Connectors included in the Arrow MAC Two-Lumen Central Venous Access Kit and the Arrow Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kit.
Reason for recall: There is the potential for inadequate connection between the top and bottom housings of the Micro Clave Clear Connectors included in the Arrow MAC Two-Lumen Central Venous Access Kit and the Arrow Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kit. Distribution: US Distributor in states of: FL, GA, KY, OH, PA and WV. Quantity: 80 units Lot/code info: UDI/DI 10801902159448, Lot Number 13F22C0349
10801902159448
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.