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Transporter 116062A0Recalls & reported problems

MAQUET GmbH · Class 1

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04046768103986), received between Jun 12, 2025 and Jun 12, 2025 — classified as 2 injuries.

The most frequently reported specific device problem is “Use of Device 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

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 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: 2 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: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520262
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Use of Device Problem2

Patient problems

  • Hernia2
  • Pain2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • InjuryJun 12, 2025Use of Device Problem; Use of Device Problem

    GETINGE BECAME AWARE OF AN EVENT WITH ONE OF OUR TRANSPORTERS - 116062A0 - TRANSPORTER USED WITH 116001D0 - OTESUS OPERATING TABLE SYSTEM, 116010B0 - UNIVERSAL TABLETOP AND 116045AC - CARBON FIBRE INSERTABLE PLATE. AS IT WAS STATED, THE ANESTHETIZED PATIENT SECURED WITH BELTS WAS LYING IN A PRONE POSITION ON A TABLE. THE TABLE WAS RAISED SLIGHTLY, AND THE POSITIONING NURSE KNELT UNDER THE TABLE AT THE HEAD END. THE DOCTOR PRESSED DOWN SLIGHTLY ON THE LEG SUPPORTS. AS A RESULT, THE TABLE DROPPED ABRUPTLY, TRAPPING THE POSITIONING NURSE. THE TABLE WAS RAISED TO RELEASE THE POSITIONING NURSE. THE NURSE HAS SUFFERED A HERNIATED DISC, REPORTED BACK PAIN AND WAS SUBSEQUENTLY SIGNED OFF SICK. THE PATIENT WAS NOT INJURED IN THE INCIDENT. THE PROCEDURE WAS SLIGHTLY DELAYED AS A RESULT. WE DECIDED TO REPORT THE EVENT DUE TO A SERIOUS INJURY OF THE USER. REF- (B)(4).

    Patient problems: Hernia; Pain

    MAUDE report 22193758 ↗
  • InjuryJun 12, 2025Use of Device Problem; Use of Device Problem

    GETINGE BECAME AWARE OF AN EVENT WITH ONE OF OUR COLUMNS - 116001D0 - OTESUS OPERATING TABLE SYSTEM USED WITH 116010B0 - UNIVERSAL TABLETOP, 116045AC - CARBON FIBRE INSERTABLE PLATE AND 116062A0 - TRANSPORTER. AS IT WAS STATED, THE ANESTHETIZED PATIENT SECURED WITH BELTS WAS LYING IN A PRONE POSITION ON A TABLE. THE TABLE WAS RAISED SLIGHTLY, AND THE POSITIONING NURSE KNELT UNDER THE TABLE AT THE HEAD END. THE DOCTOR PRESSED DOWN SLIGHTLY ON THE LEG SUPPORTS. AS A RESULT, THE TABLE DROPPED ABRUPTLY, TRAPPING THE POSITIONING NURSE. THE TABLE WAS RAISED TO RELEASE THE POSITIONING NURSE. THE NURSE HAS SUFFERED A HERNIATED DISC, REPORTED BACK PAIN AND WAS SUBSEQUENTLY SIGNED OFF SICK. THE PATIENT WAS NOT INJURED IN THE INCIDENT. THE PROCEDURE WAS SLIGHTLY DELAYED AS A RESULT. ACCORDING TO THE PROVIDED INFORMATION, THE EVENT WAS CAUSED BY A CLEAR MISUSE. WE DECIDED TO REPORT THE EVENT DUE TO A SERIOUS INJURY OF THE USER.

    Patient problems: Hernia; Pain

    MAUDE report 22192111 ↗

Other TABLE, OPERATING-ROOM, AC-POWERED devices

All TABLE, OPERATING-ROOM, AC-POWERED devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.