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