FDAJuly 24, 2020device

DABRA RA-308 Excimer Laser, SN: ******* - Product Usage: The device is intended for use in ablating a channel in occlusive peripheral vascular disease.

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

The hazard

Due to the taller wheel mounting on the laser, the laser may fall over potentially causing user or patient injury.

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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