FDANovember 25, 2024device

AURYON LASER SYSTEM 100-120 VAC. Model Number: EXM001. Product Number: EXM-2001-1100

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

The hazard

Potential for procedural delays or interruptions during use of the Auryon Atherectomy System due to the Auryon Atherectomy System not advancing to the Activation (Ready) mode.

What to do

FDA enforcement status: Ongoing

Brands named

angiodynamics

UPCs

07290017590110

Recall history

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

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