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FDAOctober 27, 2022device

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

Official recall recorded by the U.S. Food & Drug Administration.

The 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.

What to do

FDA enforcement status: Terminated

Brands named

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UPCs

10801902159448

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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