Hugo RAS MRASC0003Recalls & reported problems
Covidien LP · Tower, 120 v · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10884521850866), received between Jun 16, 2026 and Sep 17, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Application Program Freezes or Fails to Launch” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Application Program Freezes or Fails to Launch2
- Incorrect, Inadequate or Imprecise Result or Readings1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 17, 2026Application Program Freezes or Fails to Launch
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50809036 ↗MalfunctionJun 16, 2026Incorrect, Inadequate or Imprecise Result or Readings; Application Program Freezes or Fails to Launch
IT WAS REPORTED THAT DURING A DEMO/INSTALLATION ACTIVITY, THE TOWER HAD A NON-RECOVERABLE ERROR AND EXPERIENCED A COMMUNICATION ISSUE FOLLOWING SYSTEM INSTALLATION. THE ISSUE WAS IDENTIFIED AFTER INSTALLATION AND WAS RESOLVED BY REPAIRING A CABLE CONNECTION. NO PATIENT INVOLVEMENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25523611 ↗
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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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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