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FDA (Device enforcement)Recalled 2022-10-27closedclass i

ARROW INTERNATIONAL Inc.: Pressure Injectable Arrowg+ard Blue Plus Three-Lumen CVC Kit, REF numbers: a) ASK-42703-NS, b) ASK-42703-PCCH2, c) ASK-42703-PUPM1, d) ASK-45703-NS, e) ASK-45703-PAU, f) ASK-

Hazard

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.

Details from the source

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: 1275 units Lot/code info: a) ASK-42703-NS: UDI/DI 10801902162905, Lot Numbers: 13F22B0495 b) ASK-42703-PCCH2: UDI/DI 10801902141030, Lot Numbers: 13F22C0862 c) ASK-42703-PUPM1: UDI/DI 10801902159592, Lot Numbers: 13F22B0021 d) ASK-45703-NS: UDI/DI 10801902162912, Lot Numbers: 13F22C0244 e) ASK-45703-PAU: UDI/DI 10801902159110, Lot Numbers: 13F22D0121 f) ASK-45703-PCAM1: UDI/DI 10801902203158, Lot Numbers: 13F22C0553 g) ASK-45703-PCCH2: UDI/DI 10801902141047, Lot Numbers: 13F22B0641 h) ASK-45703-PN: UDI/DI 10801902140675, Lot Numbers: 13F22C0350

UPC codes

10801902162905, 10801902141030, 10801902159592, 10801902162912, 10801902159110, 10801902203158, 10801902141047, 10801902140675

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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