ARROW INTERNATIONAL Inc.: Medical Device Recall in 2022 - (Recall #: Z-0351-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

Arrow MAC Two-Lumen Central Venous Access Kit fr use with 7 - 7.5 Fr Catheters, REF ASK-11242-UPM1; catheter introducer

Product Classification:

Class I

Date Initiated: October 27, 2022

Date Posted: December 21, 2022

Recall Number: Z-0351-2023

Event ID: 91090

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.

Status: Terminated

Product Quantity: 80 units

Code Information:

UDI/DI 10801902159448, Lot Number 13F22C0349

Distribution Pattern:

US Distributor in states of: FL, GA, KY, OH, PA and WV.

Voluntary or Mandated:

Voluntary: Firm initiated