YUNO II mobile operating table 143302B0Recalls & reported problems
MAQUET GmbH · Class 1
Data updated Oct 16, 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 04046768133013), received between Jun 25, 2024 and Apr 20, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Positioning Failure” (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
- Positioning Failure2
- Failure to Interrogate1
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.
MalfunctionApr 20, 2026Positioning Failure
GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR MOBILE TABLE 143302B0 - YUNO 2 EU WITH AUTODRIVE. AS IT WAS STATED, THE TABLE BECAME STUCK IN A RAISED POSITION DURING THE PROCEDURE. THE PATIENT WAS SAFELY TRANSFERRED FROM THE ELEVATED TABLE TO A RECOVERY BED WITHOUT INCIDENT. THERE WAS NO INJURY REPORTED, HOWEVER, WE DECIDED TO REPORT THE ISSUE BASED ON THE POTENTIAL FOR SERIOUS INJURY IF THE SITUATION, NAMELY THE INABILITY TO POSITION THE TABLE AS REQUIRED DURING SURGERY, WAS TO REOCCUR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24924564 ↗MalfunctionJun 25, 2024Positioning Failure; Failure to Interrogate; Positioning Failure; Failure to Interrogate
ON 12TH JUNE 2024, GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR MOBILE TABLES - 143302B0 - YUNO 2 EU WITH AUTODRIVE. AS IT WAS STATED, THE SURGEON FINISHED THE CASE AND WANTED TO LOWER THE TABLE FROM THE MAXIMUM HEIGHT POSITION. THE TABLE WAS TOTALLY UNRESPONSIVE FROM HANDSET AND OVERRIDE PANEL AND THE ANESTHETIZED PATIENT COULD NOT BE LOWERED. THERE WAS A MESSAGE OF NO COMMUNICATION OR DATA SHOWN ON A HAND CONTROL. THE CONTROL UNIT WAS CHECKED AND IT WAS CONFIRMED THAT LED WAS FLASHING WHEN HANDSET BUTTONS WERE PRESSED. THE ISSUE RESULTED IN A DELAY. BASED ON THE EVALUATION PROVIDED BY THE TECHNICIAN, THE MALFUNCTION OF CONTROL UNIT WAS CONFIRMED. THERE WAS NO INJURY REPORTED, HOWEVER, WE DECIDED TO REPORT THE ISSUE BASED ON THE POTENTIAL FOR SERIOUS INJURY IF THE SITUATION, NAMELY THE OPERATING TABLE NOT RESPONDING TO REMOTE CONTROL OR OVERRIDE PANEL LEADING TO INABILITY TO POSITION THE TABLE DUE TO CONTROL UNIT MALFUNCTION, WAS TO REOCCUR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19605026 ↗
Other TABLE, OPERATING-ROOM, AC-POWERED devices
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- MEERA mobile operating table 720001F2MAQUET GmbH · TABLE, OPERATING-ROOM, AC-POWERED2 recalls0 reports
- HarmonyAIR A-Series Suspension SystemSteris Corporation · TABLE, OPERATING-ROOM, AC-POWERED2 recalls0 reports
- HarmonyAIR A-Series Suspension SystemSteris Corporation · TABLE, OPERATING-ROOM, AC-POWERED2 recalls0 reports
- HarmonyAIR A-Series Suspension SystemSteris Corporation · TABLE, OPERATING-ROOM, AC-POWERED2 recalls0 reports
- MEERA mobile operating table 720001B2MAQUET GmbH · TABLE, OPERATING-ROOM, AC-POWERED1 recall19 reports
- MAGNUS operating table system 118001B2MAQUET GmbH · TABLE, OPERATING-ROOM, AC-POWERED1 recall17 reports
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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