MAGNUS operating table systemRecalls & reported problems across all models
MAQUET GmbH · 8 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names at least one MAGNUS operating table system model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 39
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 1
We found 8 models of MAGNUS operating table system by MAQUET GmbH in the FDA's device registry (GUDID). Together they are named in 39 adverse event reports in the FDA's MAUDE database, received between Mar 16, 2023 and Apr 24, 2026 — classified as 39 malfunctions.
The most frequently reported specific device problem is “Positioning Failure” (20 reports).
1 FDA recall record name at least one of these models by its device 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
MAGNUS operating table system recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- 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 · names 8 of these models · Recall details · FDA record ↗
Most reported MAGNUS operating table system problems
Device problems
- Positioning Failure20
- Communication or Transmission Problem9
- Computer Software Problem6
- Use of Device Problem6
- Degraded5
- Device Sensing Problem5
- Failure to Sense5
- Positioning Problem4
Patient problems
- No Clinical Signs, Symptoms or Conditions39
MAGNUS operating table system models
8 models, most reported first. Each model has its own page with its reports, recalls and device details.
- MAGNUS operating table system 118001B2TABLE, OPERATING-ROOM, AC-POWERED1 recall17 reports
- MAGNUS operating table system 118001A0TABLE, OPERATING-ROOM, AC-POWERED1 recall6 reports
- MAGNUS operating table system 118001C0TABLE, OPERATING-ROOM, AC-POWERED1 recall5 reports
- MAGNUS operating table system 118001B1TABLE, OPERATING-ROOM, AC-POWERED1 recall4 reports
- MAGNUS operating table system 118001B4TABLE, OPERATING-ROOM, AC-POWERED1 recall4 reports
- MAGNUS operating table system 118001D0TABLE, OPERATING-ROOM, AC-POWERED1 recall2 reports
- MAGNUS operating table system 118001B0TABLE, OPERATING-ROOM, AC-POWERED1 recall1 report
- MAGNUS operating table system 118001B3TABLE, OPERATING-ROOM, AC-POWERED1 recall0 reports
Recent MAGNUS operating table system adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionApr 24, 2026Unintended Movement
GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR TABLE 118001C0 - MAGNUS TABLE COLUMN, MOBILE. AS IT WAS STATED, DURING THE POSITIONING PROCEDURE, THE ANESTHETIZED PATIENT WAS ON THE OPERATING TABLE AND ADJUSTMENTS WERE BEING MADE USING THE WIRELESS REMOTE CONTROL. WHEN THE BUTTON TO LOWER THE TABLE WAS PRESSED, THE COLUMN DID NOT EXECUTE THE COMMANDED MOVEMENT. INSTEAD, IT BEGAN TILTING TOWARD THE PATIENT¿S LEFT SIDE AND CONTINUED TO DO SO UNCONTROLLABLY, EVEN AFTER THE BUTTON WAS RELEASED. THIS CREATED A RISK OF PATIENT FALL, WHICH WAS ULTIMATELY AVOIDED. THERE WAS NO INJURY REPORTED, HOWEVER, WE DECIDED TO REPORT THE ISSUE BASED ON THE POTENTIAL FOR SERIOUS INJURY IF THE SITUATION, NAMELY UNINTENDED MOVEMENT RESULTING IN THE CHANGE OF THE PATIENT'S POSITION, WAS TO REOCCUR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24979272 ↗MalfunctionApr 8, 2026Positioning Failure
GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR COLUMNS. AS STATED, DURING A SURGICAL PROCEDURE ON A PATIENT, THE OPERATING TABLE COLUMN BECAME INOPERATIVE, EVEN WITH 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 24813036 ↗MalfunctionMar 26, 2026Device Sensing Problem
GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR TABLE 118001B4 - HYBRID OR TABLE COLUMN, SURFACE-MOUNTED. AS IT WAS STATED, DURING THE SURGERY THE DSA REPORTED AN ERROR, THE OPERATING TABLE MOVED SLOWLY, AND 3D IMAGING WAS IMPOSSIBLE. THERE WAS NO INJURY REPORTED, HOWEVER, WE DECIDED TO REPORT THE ISSUE BASED ON THE POTENTIAL FOR SERIOUS INJURY IF THE SITUATION, THE INABILITY TO POSITION THE TABLE AS REQUIRED DURING THE PROCEDURE, WAS TO REOCCUR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24697364 ↗MalfunctionMar 19, 2026Communication or Transmission Problem
GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR TABLE 118001B4 - HYBRID OR TABLE COLUMN, SURFACE-MOUNTED. AS IT WAS STATED, DURING THE SURGERY THE DSA REPORTED AN ERROR, THE OPERATING TABLE MOVED SLOWLY, AND 3D IMAGING WAS IMPOSSIBLE. THERE WAS NO INJURY REPORTED, HOWEVER, WE DECIDED TO REPORT THE ISSUE BASED ON THE POTENTIAL FOR SERIOUS INJURY IF THE SITUATION, THE INABILITY TO POSITION THE TABLE AS REQUIRED DURING THE PROCEDURE, WAS TO REOCCUR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24638025 ↗MalfunctionMar 6, 2026Device Sensing Problem
GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR TABLE 118001B4: HYBRID OR TABLE COLUMN, SURFACE-MOUNTED. AS IT WAS STATED, DURING THE EMERGENCY SURGERY INVOLVING A PATIENT WITH A RUPTURED INTRACRANIAL ANEURYSM, THE DSA REPORTED AN ERROR, THE OPERATING TABLE MOVED SLOWLY, AND 3D IMAGING WAS IMPOSSIBLE. WITH REMOTE GUIDANCE FROM THE MANUFACTURER'S ENGINEER, THE ERROR WAS TEMPORARILY RESOLVED, BUT THE SAME ERROR REAPPEARED FIVE MINUTES LATER. AFTER THE ERROR OCCURRED, THE EQUIPMENT MOVED SLOWLY, MAKING 3D SCANNING UNUSABLE AND PREVENTING THE PROVISION OF REAL-TIME 3D PATH GUIDANCE, A RECURRING CYCLE. THE SURGERY WAS FINISHED. THERE WAS NO INJURY REPORTED. HOWEVER, WE DECIDED TO REPORT THE ISSUE BASED ON THE POTENTIAL FOR SERIOUS INJURY IF THE SITUATION, NAMELY DELAY IN START OF TREATMENT IN A CRITICAL STEP OF THE TREATMENT, WAS TO REOCCUR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24530352 ↗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 ↗MalfunctionJun 18, 2025Positioning Failure; Failure to Sense; Positioning Failure; Failure to Sense
GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR COLUMNS - 118001B2 ¿ HYBRID OR TABLE COLUMN, SURFACE-MOUNTED USED WITH 118012A0 - MULTIMODALITY TRANSFER TABLE TOP EU. AS IT WAS STATED, AFTER APPROXIMATELY ONE HOUR OF ONGOING NEUROSURGICAL SURGERY, THE TABLE REPORTED ERROR 104 AND 110 ON THE IR TRANSMITTER WHEN ATTEMPTING THE TRENDELENBURG POSITION, THE OPERATING TABLE COULD ONLY BE MOVED IN THE ANTITRENDELENBURG POSITION. THE REQUIRED POSITION COULD NOT BE REACHED VIA REMOTE HAND CONTROL, AS WELL AS THE OVERRIDE PANEL AND OTHER AVAILABLE CONTROLLERS. THE CONDITION LASTED FOR SEVERAL TENS OF MINUTES, THEN THE TABLE STARTED WORKING AGAIN FOR NO APPARENT REASON. THE SURGERY WAS COMPLETED. THE GETINGE TECHNICIAN WAS UNABLE TO RE-SIMULATE THE FAULT DURING THE TEST. AFTER THE EVALUATION OF THE DOWNLOADED LOG FILES, THE ERRORS RELATED TO THE SENSOR AND COLUMN HEAD WERE FOUND. THE POSITION SENSORS IN THE OPERATING COLUMN AND TABLE TOP WERE RECALIBRATED, AND THE DEVICE WAS RESTORED TO FULL WORKING ORDER AND RETURNED TO SERVICE. 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 RES
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22267467 ↗MalfunctionSep 26, 2024Positioning Failure; Electrical /Electronic Property Problem; Positioning Failure; Electrical /Electronic Property Problem
GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR COLUMNS - 118001C0 - MAGNUS TABLE COLUMN, MOBILE. AS IT WAS STATED, THE COLUMN BROKE DOWN DURING EMERGENCY LAPAROTOMY ON THE ANESTHETIZED PATIENT. THE TABLE TOP WAS IN AN INCLINED POSITION AND THE PATIENT WAS NON-TRANSFERABLE. ACCORDING TO THE PROVIDED INFORMATION, THE TABLE COULD NOT BE OPERATED USING THE REMOTE CONTROL OR OVERRIDE PANEL AND THERE WERE NO INDICATOR LIGHTS ON THE BASE OR ON THE CONTROL PANEL WHEN THE CHARGER WAS PLUGGED IN. FOLLOWING REMOVAL AND REPLACEMENT OF THE MAIN FUSE DURING THE PROCEDURE, THE COLUMN COULD BE WOKEN UP. THE ISSUE RESULTED IN A 30-MINUTE DELAY. THERE WAS NO INJURY REPORTED, HOWEVER, WE DECIDED TO REPORT THE ISSUE BASED ON THE POTENTIAL FOR SERIOUS INJURY IF THE SITUATIONS, NAMELY THE OPERATING TABLE NOT RESPONDING TO THE REMOTE CONTROL OR OVERRIDE PANEL LEADING TO THE INABILITY TO POSITION THE TABLE AND PROCEDURAL DELAY DURING THE EMERGENCY SURGERY, WERE TO REOCCUR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20308980 ↗MalfunctionAug 14, 2024Positioning Failure; Failure to Interrogate; Positioning Failure; Failure to Interrogate
GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR COLUMNS - 118001C0 - MAGNUS TABLE COLUMN, MOBILE. AS IT WAS STATED, THE TABLE COLUMN STOPPED AND COULD NOT BE OPERATED WITH ANY CONTROLS. THE SURGERY WAS DELAYED BY 20 MINUTES. DUE TO THE ISSUE, IT WAS NECESSARY TO REMOVE THE ANESTHETIZED PATIENT FROM THE OPERATING TABLE AFTER THE PROCEDURE WAS COMPLETED. ACCORDING TO THE PROVIDED INFORMATION, THE OVERRIDE PANEL DID NOT WORK EVEN WHEN THE DEVICE WAS CONNECTED TO AC POWER. AFTER SWITCHING THE FUSE OFF AND BACK ON, THE EQUIPMENT STARTED WORKING AGAIN. 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 OVERRIDE PANEL, LEADING TO THE INABILITY TO POSITION THE TABLE DURING SURGERY, WAS TO REOCCUR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19979120 ↗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 ↗MalfunctionJun 5, 2024Computer Software Problem; Adverse Event Without Identified Device or Use Problem; Positioning Problem; Computer Software Problem; Adverse Event Without Identified Device or Use Problem; Positioning Problem
ON 22ND MAY 2024, GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR COLUMNS 9118001B1 HYBRID OR TABLE COLUMN, SURFACE-MOUNTED. AS IT WAS STATED, THERE WAS AN INTERNAL COMMUNICATION ISSUE WITH THE TABLE CONTROLS - NOT ACKNOWLEDGING BREAK SYSTEM AND NOT RECOGNIZING THE TABLE. THE USE OF THE TABLE WAS LIMITED WHAT LED TO AN 1 HOUR DELAY IN CRITICAL HEART SURGERY ON THE ANESTHETIZED PATIENT. EVENTUALLY, THE SURGERY HAD TO BE RESCHEDULED. THE CUSTOMER TESTED THE GENERATORS AND CONCLUDED THAT SEVERAL PIECES OF EQUIPMENT HAD TROUBLE AFTERWARDS. THE TABLE REQUIRED A HARD RESET INVOLVING REMOVING TABLE POWER AND RESTARTING IT. FOLLOWING SERVICE VISIT ON SITE IT WAS CONFIRMED THAT THE PROBLEM WAS FIXED WITH THE HARD RESET. 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 OR POSTPONEMENT OF CRITICAL SURGERY RESULTING IN PROLONGED ANESTHESIA TIME, WAS TO REOCCUR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19465422 ↗MalfunctionApr 24, 2024Positioning Failure; Positioning Failure
ON (B)(6) 2024, GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR COLUMNS - 118001C0 - MAGNUS TABLE COLUMN, MOBILE. AS IT WAS STATED, THE USER REPORTED ERRORS 96 AND 107 RELATED TO OVERCURRENT. FOLLOWING A SERVICE VISIT ON SITE, THE ISSUE WAS CONFIRMED. THE COLUMN WAS BLOCKED AND DID NOT MOVE UP/ DOWN DUE TO MALFUNCTION OF HYDRAULIC UNIT. ON (B)(6) 2024, ADDITIONAL INFORMATION HAS BEEN RECEIVED. AS IT WAS STATED, THE TABLE REMAINED BLOCKED WITH THE PATIENT IN EXTREME TILT AND ANTI-TRENDELENBURG POSITION. THE COLUMN DID NOT RESPOND TO COMMANDS TO BRING THE TABLE TOP TO "0" POSITION AND THE EMERGENCY SYSTEM DID NOT WORK. AS A RESULT, THE INTERVENTION WAS COMPLETED IN NON-ERGONOMIC POSITION AND INTUBATED PATIENT HAD TO BE TRANSFERRED MANUALLY TO THE HOSPITAL BED AT THE END OF SURGERY. 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 PROCEDURE DUE TO THE MALFUNCTION OF HYDRAULIC UNIT, WAS TO REOCCUR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19171875 ↗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 ↗MalfunctionMar 28, 2024Failure to Sense; Communication or Transmission Problem; Air/Gas in Device; Failure to Sense; Communication or Transmission Problem; Air/Gas in Device
ON 25TH MARCH 2024, GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR COLUMNS - 118001B1 - HYBRID OR TABLE COLUMN, SURFACE-MOUNTED. AS IT WAS STATED, THE CONNECTION WITH THE ANGIOGRAPHY DEVICE (PHILIPS AZURION 7 M20) WAS INTERRUPTED DURING SURGERY. THE PATIENT WAS ALREADY UNDER ANESTHESIA. DUE TO THE ISSUE, THE INCISION HAD TO BE CLOSED, THE SURGERY WAS INTERRUPTED AND RESCHEDULED TO THREE DAYS LATER. THE TECHNICIAN INDICATED THAT THE AIR WAS MIXED IN THE VERTICAL TILT CYLINDER CAUSING THE SENSOR VALUES TO BECOME UNSTABLE. THERE WAS NO INJURY REPORTED, HOWEVER, WE DECIDED TO REPORT THE ISSUE BASED ON THE POTENTIAL FOR SERIOUS INJURY IF THE SITUATION, NAMELY THE RESCHEDULING OF THE SURGERY ON THE ALREADY ANESTHETIZED PATIENT, WAS TO REOCCUR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18990020 ↗MalfunctionMar 20, 2024Positioning Failure; Positioning Failure
ON 13TH MARCH 2024, GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR COLUMNS - 118001D0 - MAGNUS OR-TABLE COLUMN, INDEPEN. AS IT WAS STATED, THE OPERATING TABLE COULD NO LONGER BE MOVED TO 0 POSITION FROM THE LATERAL TILTING OF THE TABLE DURING A SURGERY ON AN ANESTHETIZED PATIENT. THE MOTORS COULD BE HEARD VERY QUIETLY, HOWEVER, THERE WAS NO MOVEMENT IN THE MODULES. IF THE MODULES WERE CONTROLLED SEPARATELY, THEY WORKED WITH A DELAY. NO ERROR MESSAGE WAS DISPLAYED ON THE REMOTE CONTROL. THE EMERGENCY PANEL DID NOT WORK AS WELL. AFTER APPROXIMATELY 10 MINUTES FROM THE LAST MANEUVER, THE TILTING COULD BE CANCELLED BY REMOTE CONTROL, HOWEVER, IT WAS STILL IMPOSSIBLE TO MOVE THE TABLE INTO 0 POSITION. AT THE TIME OF INCIDENT, THE TABLE BASE WAS CONNECTED TO THE POWER SUPPLY. THE ISSUE RESULTED IN A DELAY AS THE PATIENT COULD NOT BE POSITIONED PROPERLY. THERE WAS NO INJURY REPORTED, HOWEVER, WE DECIDED TO REPORT THE ISSUE BASED ON THE POTENTIAL FOR SERIOUS INJURY IF SITUATIONS, NAMELY OPERATING TABLE NOT RESPONDING TO REMOTE CONTROL NOR OVERRIDE PANEL LEADING TO INABILITY TO POSITION THE PATIENT AS REQUIRED AND THE DELAY IN SURGERY RESULTING IN PROLONGED ANESTHESIA TIME, WERE TO REOCCU
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18941432 ↗
Other MAQUET GmbH products
- MEERA mobile operating table3 models · 32 reports · 4 recalls
- ALPHAMAXX mobile operating table3 models · 8 reports · 3 recalls
- MEERA ST mobile operating table3 models · 1 reports · 3 recalls
- MEERA CL mobile operating table2 models · 1 reports · 2 recalls
- CORIN mobile operating table6 models · 9 reports · 1 recall
- OTESUS operating table system3 models · 20 reports
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- 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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