CORIN mobile operating table 770001B2Recalls & 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
- 2
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 04046768145207), received between Dec 5, 2024 and Jul 8, 2026 — classified as 2 injuries, 4 malfunctions.
The most frequently reported specific device problem is “Positioning Failure” (4 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
Recalls naming this device
- 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 · FDA record ↗
Most reported problems
Device problems
- Positioning Failure4
- Device Tipped Over2
- Complete Loss of Power1
- Computer Software Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
- Crushing Injury2
Recent adverse event reports
The 6 most recent of 6 reports, 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 ↗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 ↗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 ↗
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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.