Ra Medical Systems Inc: Medical Device Recalls in 2019

Updated on March 25, 2026.

According to to data from the FDA, there was 1 medical device recall made by Ra Medical Systems Inc in 2019. See the detail of the recall below.

You can see similar recalls for other firms.

Data Source: FDA.

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The DABRA Laser (model RA-308) is designed to provide ultraviolet laser energy endovascularly through a catheter to occluded lesions in the peripheral arteries to cross them. The system is a self-contained unit that consists of a light source unit and a single use catheter. The light source contains a microprocessor with software to provide safety features and a user-friendly interface. The laser operates by producing a high current discharge within a chamber that is filled with rare gases and halogen. The discharge produces pulses of UV light, which is amplified by reflecting the energy within the resonating chamber many times. The output is directed to the desired target location by the catheter. A footswitch connected to the light source controls the laser action.