Hugo RAS MRASC0002Recalls & reported problems
Covidien LP · Arm Cart Assembly · Class 2
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10884521850880), received between Aug 13, 2026 and Sep 17, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Communication or Transmission 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Communication or Transmission Problem2
- Display or Visual Feedback Problem2
- No Apparent Adverse Event2
- Unintended Collision2
- Application Program Freezes or Fails to Launch1
- Failure to Calibrate1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 17, 2026Failure to Calibrate; Application Program Freezes or Fails to Launch
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50808981 ↗MalfunctionAug 13, 2026Display or Visual Feedback Problem; Unintended Collision; Communication or Transmission Problem; No Apparent Adverse Event
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50243242 ↗MalfunctionAug 13, 2026Display or Visual Feedback Problem; Unintended Collision; Communication or Transmission Problem; No Apparent Adverse Event
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50243133 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.