Hugo RAS MRASC0001Recalls & reported problems
Covidien LP · Surgeon Console · Class 2
All models of Hugo RAS (10)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10884521850859), received between Jul 6, 2026 and Sep 17, 2026 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Activation Problem” (2 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Activation Problem2
- Application Program Freezes or Fails to Launch2
- Delayed Program or Algorithm Execution1
- Failure to Calibrate1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 17, 2026Application Program Freezes or Fails to Launch; Activation Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50808949 ↗MalfunctionSep 8, 2026Failure to Calibrate; Application Program Freezes or Fails to Launch
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50676279 ↗MalfunctionAug 4, 2026Delayed Program or Algorithm Execution
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50136387 ↗MalfunctionJul 6, 2026Activation Problem
IT WAS REPORTED THAT DURING A ROBOTIC LAPAROSCOPIC RETROPUBIC RADICAL PROSTATECTOMY WITH BILATERAL PELVIC LYMPHADENECTOMY, WHILE MOBILIZING THE PROSTATE, THE RIGHT-HAND TRIGGER ON THE SURGEON CONSOLE (SC) FELT STIFF, RESULTING IN DIFFICULTY CLUTCHING. THE SURGEON WAS ABLE TO USE THE FOOT PEDAL FOR CLUTCHING TO COMPLETE THE PROCEDURE. THERE WAS NO PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25727439 ↗
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- Hugo RAS MRASC0002Covidien LP · Modular electromechanical surgical system3 reports
- Versius Camera Head (compatible with vLimeLite) 90911Cmr Surgical Limited · Modular Electromechanical Surgical System3 reports
- Hugo RAS MRASC0003Covidien LP · Modular electromechanical surgical system2 reports
- Hugo RAS MRASI0001Covidien LP · Modular electromechanical surgical system1 report
- Hugo RAS MRASI0001Covidien LP · Modular electromechanical surgical system1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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