MODUEVO MODUEVO-MARecalls & reported problems
Maquet (Suzhou) Co. LTD · Medical Ceiling Supply Units · Class 1
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 06970283130982), received between Jan 23, 2025 and Jan 23, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Difficult or Delayed Positioning” (1 report).
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
- Difficult or Delayed Positioning1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 23, 2025Difficult or Delayed Positioning; Difficult or Delayed Positioning
ON JAN. 6TH, 2025, GETINGE SUZHOU BECAME AWARE OF A COMPLAINT REPORTED FROM THE HOSPITAL IN SWITZERLAND THAT THE CEILING COVER OF THE MODUEVO-MA IN INTENSIVE CARE ROOM 172 FELL OFF, HITTING HEAD OF A PATIENT. THE PATIENT ONLY SUFFERED A SMALL HEAD INJURY AND A SHOCK. NO MEDICAL TREATMENT WAS GIVEN AS ONLY A SMALL HEADACHE, AND THE PATIENT HAS BEEN FULLY RECOVERED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21226112 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.