CORIN mobile operating tableRecalls & reported problems across all models
MAQUET GmbH · 6 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names at least one CORIN mobile operating table model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 9
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls
- 1
We found 6 models of CORIN mobile operating table by MAQUET GmbH in the FDA's device registry (GUDID). Together they are named in 9 adverse event reports in the FDA's MAUDE database, received between Dec 5, 2024 and Jul 8, 2026 — classified as 2 injuries, 7 malfunctions.
The most frequently reported specific device problem is “Positioning Failure” (7 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
CORIN mobile operating table 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.
- Jul 14, 2025Open, Classified
Under certain conditions, such as the simultaneous use of the operating table with other medical devices, including high-frequency (HF) surgical equipment, interference may occur that could prevent the device from performing as intended. If the issue occurs, the operating table is unresponsive to command from both the universal remote control and override panel.
Z-2420-2025 · Root cause: Under Investigation by firm · names 6 of these models · Recall details · FDA record ↗
Most reported CORIN mobile operating table problems
Device problems
- Positioning Failure7
- Device Tipped Over2
- Complete Loss of Power1
- Computer Software Problem1
- Failure to Interrogate1
Patient problems
- No Clinical Signs, Symptoms or Conditions7
- Crushing Injury2
CORIN mobile operating table models
6 models, most reported first. Each model has its own page with its reports, recalls and device details.
- CORIN mobile operating table 770001B2Table, Operating-Room, Ac-Powered1 recall6 reports
- CORIN mobile operating table 770001A2Table, Operating-Room, Ac-Powered1 recall3 reports
- CORIN mobile operating table 770001A0Table, Operating-Room, Ac-Powered1 recall0 reports
- CORIN mobile operating table 770001B0Table, Operating-Room, Ac-Powered1 recall0 reports
- CORIN mobile operating table 770001F0Table, Operating-Room, Ac-Powered1 recall0 reports
- CORIN mobile operating table 770001F2Table, Operating-Room, Ac-Powered1 recall0 reports
Recent CORIN mobile operating table adverse event reports
The 9 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionJul 8, 2026Positioning Failure
GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR TABLE 770001B2 - CORIN MOBILE OPERATING TABLE. AS IT WAS STATED, DURING THE A PARTIAL NEPHRECTOMY, THE TABLE COULD NO LONGER BE TILTED, IT BECAME STUCK AND NO MOVEMENT WAS POSSIBLE. THE PATIENT HAD TO BE REPOSITIONED, AND THE TABLE HAD TO BE REMOVED FROM THE OPERATING ROOM. THIS CAUSED A DELAY OF APPROXIMATELY 20 MINUTES. THERE WAS NO INJURY REPORTED, HOWEVER, WE DECIDED TO REPORT THE ISSUE BASED ON THE POTENTIAL FOR SERIOUS INJURY IF THE SITUATION, NAMELY INABILITY TO POSITION THE TABLE DURING PROCEDURE, WAS TO REOCCUR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25746122 ↗InjuryMay 21, 2026Device Tipped Over
GETINGE BECAME AWARE OF AN ISSUE INVOLVING ONE OF OUR TABLES ¿ 770001B2 CORIN MOBILE OPERATING TABLE. WHILE PUSHING A TABLE TO THE SIDE OF THE THEATRE, THE BASE OF THE TABLE CAUGHT THE NURSE¿S FOOT, INJURING HER BIG TOE. THE NURSE ATTENDED THE EMERGENCY DEPARTMENT, WHERE THE TOE WAS CLEANED AND DRESSED. SHE WAS ADVISED THAT SHE IS LIKELY TO LOSE THE TOENAIL COMPLETELY, AS IT WAS PARTIALLY TORN FROM THE NAIL BED. NO OTHER INJURIES WERE REPORTED. WE HAVE DECIDED TO REPORT THE ISSUE DUE TO THE SERIOUS INJURY SUSTAINED BY THE USER.
Patient problems: Crushing Injury
MAUDE report 25242349 ↗InjuryMay 21, 2026Device Tipped Over
GETINGE BECAME AWARE OF AN ISSUE INVOLVING ONE OF OUR TABLES ¿ 770001B2 CORIN MOBILE OPERATING TABLE. WHILE PUSHING A TABLE TO THE SIDE OF THE THEATRE, THE BASE OF THE TABLE CAUGHT THE NURSE¿S FOOT, INJURING HER BIG TOE. THE NURSE ATTENDED THE EMERGENCY DEPARTMENT, WHERE THE TOE WAS CLEANED AND DRESSED. SHE WAS ADVISED THAT SHE IS LIKELY TO LOSE THE TOENAIL COMPLETELY, AS IT WAS PARTIALLY TORN FROM THE NAIL BED. NO OTHER INJURIES WERE REPORTED. WE HAVE DECIDED TO REPORT THE ISSUE DUE TO THE SERIOUS INJURY SUSTAINED BY THE USER.
Patient problems: Crushing Injury
MAUDE report 25239095 ↗MalfunctionMar 9, 2026Positioning Failure
GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR OPERATING TABLE 770001B2 - CORIN MOBILE OPERATING TABLE. DURING THE REVERSE TRENDELENBURG MOVEMENT, THE TABLE STOPPED IN A TILTED POSITION AND COULD NO LONGER BE OPERATED, INCLUDING THROUGH THE OVERRIDE MODE. DUE TO THE LOSS OF TABLE FUNCTIONALITY, THE CLINICAL STAFF REMOVED THE PATIENT FROM THE TABLE AND CONTINUED THE PROCEDURE USING ANOTHER OPERATING TABLE. WE DECIDED TO REPORT THE ISSUE BASED ON THE POTENTIAL FOR SERIOUS INJURY IF THE SITUATION, NAMELY INABILITY TO POSITION THE TABLE DURING PROCEDURE, WAS TO REOCCUR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24549929 ↗MalfunctionJun 6, 2025Positioning Failure; Positioning Failure
GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR MOBILE TABLES - 770001A2 - CORIN W AUTODRIVE, IPC, EU. AS IT WAS STATED, THE OPERATING TABLE STOPPED WORKING AND WAS NOT RESPONDING TO THE IR AND CABLE REMOTE CONTROLS AS WELL AS THE OVERRIDE PANEL AT THE BEGINNING OF THE COLECTOMY SURGERY. THE TABLE ALSO DID NOT WORK WHEN CONNECTED TO THE MAINS. THE PATIENT HAD TO BE MOVED TO ANOTHER OPERATING TABLE, WHICH RESULTED IN PROLONGED ANESTHESIA TIME. 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 22157422 ↗MalfunctionMay 23, 2025Positioning Failure; Failure to Interrogate; Positioning Failure; Failure to Interrogate
MANUFACTURER'S REFERENCE NUMBER (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22077628 ↗MalfunctionMay 22, 2025Positioning Failure; Complete Loss of Power; Positioning Failure; Complete Loss of Power
GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR MOBILE TABLES - 770001B2 CORIN W AUTODRIVE, SFC, EU. DURING A SHOULDER SURGERY ON AN ANESTHETIZED PATIENT, THE OPERATING TABLE BECAME UNRESPONSIVE TO THE REMOTE CONTROL DUE TO A POWER FAILURE. DESPITE PLUGGING THE OR TABLE INTO THE MAINS, THE TABLE REMAINED INOPERATIVE. EMERGENCY PROCEDURES WERE FOLLOWED TO REMOVE AND REPLACE THE TABLE. THE SURGERY RESUMED AFTER A 10 MINUTE DELAY, WHICH DID NOT OCCUR DURING A CRITICAL STEP OF 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 INABILITY TO REPOSITION THE PATIENT CAUSED BY THE OPERATING TABLE'S POWER FAILURE, WAS TO REOCCUR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22068108 ↗MalfunctionApr 17, 2025Positioning Failure; Positioning Failure
MANUFACTURER'S REFERENCE NUMBER (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21856853 ↗MalfunctionDec 5, 2024Computer Software Problem; Positioning Failure; Computer Software Problem; Positioning Failure
GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR MOBILE TABLES - 770001B2 - CORIN W AUTODRIVE, SFC, EU. AS IT WAS STATED, ALL FUNCTIONS STOPPED WORKING AND THE TABLE COULD NOT BE LEVELLED VIA HAND CONTROL OR OVERRIDE PANEL DURING SURGERY. THE TABLE WAS IN NORMAL ORIENTATION WITH FULL LONGITUDINAL SHIFT TO THE FOOT SITE, 20 DEGREES OF TRENDELENBURG AND 3 DEGREES OF RIGHT LATERAL TILT APPLIED AND COLUMN AT THE LOWEST PERMITTED HEIGHT FOR THIS TABLE TOP POSITION. FOLLOWING SERVICE VISIT ON SITE, IT WAS CONFIRMED THAT NO MOVEMENT OCCURS WHEN THE ¿0¿ OR ¿LEFT LATERAL TILT¿ BUTTONS ON THE REMOTE CONTROL OR ¿LEFT LATERAL TILT¿ AND ¿POWER¿ BUTTONS ON THE OVERRIDE PANEL ARE BEING PRESSED. THE WARNING LIGHTS WENT AMBER AND THERE WAS AUDIBLE TONE. THE TABLE WAS FULLY CHARGED AND HAND CONTROL IR WAS NOT SHOWING LOW BATTERY. 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 PATIENT DURING PROCEDURE, WAS TO REOCCUR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20851507 ↗
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
- MAGNUS operating table system8 models · 39 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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