FDAOctober 16, 2020device

DABRA Laser (RA-308 Excimer Laser) Intended Use: For use in ablating a channel in occlusive peripheral vascular disease. Indications: For crossing chronic total occlusions in patients with symptomatic infrainguinal lower extremity vascular disease.

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

The hazard

Due to footswitch not meeting required specification for protection from ingress of solids or liquids. If spilling of liquids near or on the footswitch, it may fail in the 'on' position and allow the laser to continue to lase.

What to do

FDA enforcement status: Terminated

Brands named

ra medical systems

Recall history

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

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DABRA Laser (RA-308 Excimer Laser) Intended Use: For use in ablating a channel in occlusive peripheral vascular disease. Indications: For crossing chronic total occlusions in patients with symptomatic infrainguinal lower extremity vascular disease. — Recall Details · AllClear