FDAJanuary 24, 2022device

1. Arterial Line Kit 20ga x 6" 2. Arterial Line Kit /1 20ga x 6"

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

The hazard

Guidewire included with two lots of Arterial Line Kits would not fit through the needle of the same kit. This could potentially lead to a slight delay in the procedure and minor blood loss.

What to do

FDA enforcement status: Ongoing

Brands named

argon medical devicesargonargon medical

Recall history

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

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