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ARROW INTERNATIONAL Inc. recalls Arrow MAC Two-Lumen Central Venous Access Kit fr use with 7 - 7.5 Fr Catheters, REF ASK-11242-UPM1; catheter introducer
Recalled December 21, 2022 · FDA recall Z-0351-2023 · ARROW INTERNATIONAL
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. · FDA Class I
Units
80 units
Sold at
US Distributor in states of: FL, GA, KY, OH, PA and WV.
Description
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.
Product
Arrow MAC Two-Lumen Central Venous Access Kit fr use with 7 - 7.5 Fr Catheters, REF ASK-11242-UPM1; catheter introducer
Manufacturer(s)
ARROW INTERNATIONAL Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →