FDAJanuary 23, 2020device

DABRA Laser (RA-308 Excimer Laser). The DABRA Laser and DABRA Catheter is an excimer laser ultraviolet light source and delivery system, collectively the DABRA Laser System". The system is designed to deliver the energy to the surgical site to ablate unwanted material. The optical conduit is used...

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

The hazard

A software issue was identified which could result in user or patient injury, or may adversely impact laser performance. It is possible that an unintended release of laser light (radiation) may occur, injuring the user or patient.

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). The DABRA Laser and DABRA Catheter is an excimer laser ultraviolet light source and delivery system, collectively the DABRA Laser System". The system is designed to deliver the energy to the surgical site to ablate unwanted material. The optical conduit is used... — Recall Details · AllClear