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MAGNUS operating table system 118001A0Recalls & reported problems

MAQUET GmbH · Class 1

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
6
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 04046768031500), received between Nov 29, 2023 and Nov 21, 2025 — classified as 6 malfunctions.

The most frequently reported specific device problem is “Positioning Failure” (6 reports).

1 FDA recall record name this device's identifier, 1 still open.

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: 1 reportsDec 2023: 0 reportsJan 2024: 2 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 1 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 1 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: 1 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.

Recalls naming this device

  1. Feb 11, 2021Open, Classified

    There is a potential for hydraulic leakage at the inclination function to occur resulting in an unintended Trendelenburg or anti-Trendelenburg movement of the table top depending on patient positioning which may lead to the patient having to be transferred to another OR table causing a delay in the procedure.

    Z-1296-2021 · Root cause: Device Design · FDA record ↗

Most reported problems

Device problems

  • Positioning Failure6
  • Circuit Failure2
  • Failure to Conduct2
  • Misconnection2
  • Positioning Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions6

Recent adverse event reports

The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

  • MalfunctionNov 21, 2025Positioning Failure; Positioning Failure

    GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR COLUMNS ¿ 118001A0 ¿ MAGNUS TABLE COLUMN FOR BUILT-IN PLATE. AS STATED, DURING A SURGICAL PROCEDURE ON A PATIENT IN CRITICAL CONDITION, THE OPERATING TABLE COLUMN BECAME INOPERATIVE - BOTH THE CONTROL PANEL AND THE REMOTE CONTROL WERE NON-FUNCTIONAL. THE MALFUNCTION RESULTED IN THE TRANSFER OF THE PATIENT TO ANOTHER OPERATING ROOM. 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 THE REMOTE CONTROL OR THE OVERRIDE PANEL, LEADING TO INABILITY TO POSITION THE PATIENT AS REQUIRED, WAS TO REOCCUR.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23617776 ↗
  • MalfunctionAug 6, 2024Circuit Failure; Positioning Failure; Circuit Failure; Positioning Failure

    ON 20TH JUNE 2024, GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR COLUMNS - 118001A0 - MAGNUS TABLE COLUMN FOR BUILT-IN PLATE. INITIALLY PROVIDED INFORMATION SUGGESTED COLUMN FAILURE. ON 31ST JULY 2024, ADDITIONAL INFORMATION HAS BEEN RECEIVED. AS IT WAS STATED, THE ISSUE OCCURRED DURING PLANNED CARDIAC SURGERY ON THE ANESTHETIZED PATIENT. NO MOVEMENT WAS POSSIBLE USING REMOTE CONTROL AS WELL AS OVERRIDE PANEL, PREVENTING THE PATIENT FROM BEING POSITIONED FOR THE PLANNED PROCEDURE. THE PATIENT WAS TRANSFERRED TO ANOTHER OPERATING ROOM. THERE WAS NO INJURY REPORTED, HOWEVER, WE DECIDED TO REPORT THE ISSUE BASED ON THE POTENTIAL FOR SERIOUS INJURY IF THE SITUATION, NAMELY OPERATING TABLE NOT RESPONDING TO REMOTE CONTROL NOR OVERRIDE PANEL LEADING TO INABILITY TO POSITION THE PATIENT AS REQUIRED AND RESULTING IN TRANSFER TO ANOTHER OPERATING ROOM, WAS TO REOCCUR.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 19917864 ↗
  • MalfunctionApr 11, 2024Positioning Failure; Positioning Failure

    ON 27TH MARCH 2024,, GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR COLUMNS - 118001A0 - MAGNUS TABLE COLUMN FOR BUILT-IN PLATE. AS IT WAS STATED, THE TABLE TOP COULD NOT BE LIFTED BY THE COLUMN WHILE THE ANESTHETIZED PATIENT WAS ON THE TABLE. THE PROBLEM RESULTED IN A SMALL DELAY IN START OF SURGERY. BASED ON THE INFORMATION PROVIDED BY THE GETINGE TECHNICIAN FOLLOWING SERVICE VISIT ON SITE, THE ISSUE WITH HYDRAULIC UNIT WAS FOUND. THERE WAS NO INJURY REPORTED, HOWEVER, WE DECIDED TO REPORT THE ISSUE BASED ON THE POTENTIAL FOR SERIOUS INJURY IF THE SITUATION, NAMELY THE DELAY IN SURGERY RESULTING IN PROLONGED ANESTHESIA TIME, WAS TO REOCCUR.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 19086124 ↗
  • MalfunctionJan 23, 2024Failure to Conduct; Positioning Failure; Misconnection; Failure to Conduct; Positioning Failure; Misconnection

    ON 10TH JANUARY 2024 GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR COLUMNS - 118001A0 - MAGNUS TABLE COLUMN FOR BUILT-IN PLATE. AS IT WAS STATED, AT THE END OF PROCEDURE, THE OPERATING TABLE TOP WAS NO LONGER RECOGNIZED CORRECTLY DUE TO DAMAGED CONTACT MODULE ON THE COLUMN. THE ISSUE LED TO A DELAY IN OPERATION ON THE ANESTHETIZED PATIENT. THE PATIENT HAD TO BE MOVED TO ANOTHER OPERATING TABLE FOLLOWING THE PROCEDURE. THE INCIDENT WAS INITIALLY ASSESSED AS REPORTABLE DUE TO A DELAY IN SURGERY RESULTING IN PROLONGED ANESTHESIA TIME. RECENTLY, THE INCIDENT HAS BEEN REEVALUATED AS ACCORDING TO THE MEDICAL EXPERT'S ASSESSMENT, THE PROCEDURAL DELAY DID NOT HAVE ANY MAJOR CLINICAL RELEVANCE IN THIS SITUATION. THE SCENARIO DESCRIBED IN THE RECORD IS CONSIDERED AS NON-REPORTABLE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18562077 ↗
  • MalfunctionJan 23, 2024Failure to Conduct; Positioning Failure; Misconnection; Failure to Conduct; Positioning Failure; Misconnection

    ON (B)(6) 2024 GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR COLUMNS - 118001A0 - MAGNUS TABLE COLUMN FOR BUILT-IN PLATE. AS IT WAS STATED, AT THE END OF PROCEDURE, THE OPERATING TABLE TOP WAS NO LONGER RECOGNIZED CORRECTLY DUE TO DAMAGED CONTACT MODULE ON THE COLUMN. THE ISSUE LED TO A DELAY IN OPERATION ON THE ANESTHETIZED PATIENT. THE PATIENT HAD TO BE MOVED TO ANOTHER OPERATING TABLE FOLLOWING THE PROCEDURE. THERE WAS NO INJURY REPORTED, HOWEVER, WE DECIDED TO REPORT THE ISSUE BASED ON THE POTENTIAL FOR SERIOUS INJURY IF THE SITUATION, NAMELY THE DELAY IN SURGERY RESULTING IN PROLONGED ANESTHESIA TIME, WAS TO REOCCUR.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18562076 ↗
  • MalfunctionNov 29, 2023Circuit Failure; Positioning Failure; Positioning Problem; Circuit Failure; Positioning Failure; Positioning Problem

    ON (B)(3) 2023 GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR TABLE COLUMNS ¿118001A0 - MAGNUS TABLE COLUMN FOR BUILT-IN PLATE. AS IT WAS STATED, DURING THE SURGERY OF THE ANESTHETIZED PATIENT, THE LONGITUDINAL DISPLACEMENT CONNECTION WITH THE TABLE TOP WAS LOST. THE STAFF TRIED TO MOVE THE TABLE TO THE DESIRED POSITION WHAT RESULTED IN DELAY IN TREATMENT (AROUND 2 MINUTES). THE SURGERY WAS PERFORMED UNDER DIFFICULT CONDITIONS. THERE WAS NO INJURY REPORTED, HOWEVER, WE DECIDED TO REPORT THE ISSUE BASED ON THE POTENTIAL FOR SERIOUS INJURY IF THE SITUATION, NAMELY THE DELAY IN SURGERY RESULTING IN PROLONGED ANESTHESIA TIME, WAS TO REOCCUR.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18225426 ↗

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.