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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

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 1 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 1 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

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 ↗

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Sources and updates

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