MalfunctionPZP
HYDROS HANDPIECE
Received Jan 26, 2026 · Event occurred Jan 12, 2026
Report 24177206 · MDR key 24177206
Device
Generic name
Fluid Jet Removal System
Manufacturer
Procept Biorobotics CorporationModel number
HH1000Lot number
25C03802
Patient
74 YR · Male
- No Clinical Signs, Symptoms or Conditions
Narrative
Description of Event or Problem
JUST AS DOCTOR WAS ABOUT TO DO THE CALIBRATION OF THE AQUABLATION HAND PIECE WE REALIZED THAT THE DEVICE WAS SHOWING BLANK ON THE SCREEN. THIS WAS WHEN THE DEVICE WAS STILL IN THE PATIENT'S URETHRA. DEVICE WAS REPLACED WITH ANOTHER ONE AND MED WATCH REPORT WAS MADE. NO PATIENT SAFETY CONCERN AND NO GENERAL SAFETY CONCERN.