Basic table top 118010A0Recalls & reported problems

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 04046768031593), received between Dec 28, 2023 and May 21, 2025 — classified as 2 injuries, 5 malfunctions.

The most frequently reported specific device problem is “Positioning Failure” (3 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.

Most reported problems

Recent adverse event reports

The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.

• InjuryMay 21, 2025Adverse Event Without Identified Device or Use Problem; Patient Device Interaction Problem; Adverse Event Without Identified Device or Use Problem; Patient Device Interaction Problem

  GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR TABLETOPS ¿ 118010A0 BASIS TABLETOP, INDIVIDUAL CONFIGURATION. DURING A 4-HOUR CARDIAC SURGERY, THE PATIENT WAS PLACED IN A SUPINE POSITION, AND A STAGE II PRESSURE SORE DEVELOPED ON THE BUTTOCKS. THERE WAS NO MALFUNCTION OF THE TABLETOP OR TABLE PAD, THE INJURY RESULTED FROM PROLONGED ISCHEMIA TIME AND THE PATIENT¿S GENERAL CONDITION. THE INJURY WAS DESCRIBED AS SIGNIFICANT, REQUIRING ADDITIONAL TREATMENT, EXTENDED HOSPITAL STAY, AND POSSIBLY SURGICAL INTERVENTION. WE DECIDED TO REPORT THE ISSUE DUE TO THE SERIOUS INJURY OF THE PATIENT. (B)(4).

  Patient problems: Localized Skin Lesion

  MAUDE report 22059901 ↗
• InjuryMay 21, 2025Adverse Event Without Identified Device or Use Problem; Patient Device Interaction Problem; Adverse Event Without Identified Device or Use Problem; Patient Device Interaction Problem

  GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR TABLETOPS ¿ 118010A0 BASIS TABLETOP, INDIVIDUAL CONFIGURATION. DURING A 4-HOUR CARDIAC SURGERY, THE PATIENT WAS PLACED IN A SUPINE POSITION, AND A STAGE II PRESSURE SORE DEVELOPED ON THE BUTTOCKS. THERE WAS NO MALFUNCTION OF THE TABLETOP OR TABLE PAD, THE INJURY RESULTED FROM PROLONGED ISCHEMIA TIME AND THE PATIENT¿S GENERAL CONDITION. THE INJURY WAS DESCRIBED AS SIGNIFICANT, REQUIRING ADDITIONAL TREATMENT, EXTENDED HOSPITAL STAY, AND POSSIBLY SURGICAL INTERVENTION. WE DECIDED TO REPORT THE ISSUE DUE TO THE SERIOUS INJURY OF THE PATIENT.

  Patient problems: Localized Skin Lesion

  MAUDE report 22058739 ↗
• MalfunctionMay 28, 2024Positioning Failure; Failure to Sense; Positioning Failure; Failure to Sense

  ON 13TH MAY 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 ERROR 10/105 WAS DISPLAYED AND COLUMN COULD NOT BE OPERATED WITH THE REMOTE CONTROL OR OVERRIDE PANEL DURING SURGERY ON THE ANESTHETIZED PATIENT. THE ISSUE DID NOT LEAD TO A DELAY. THE ERROR 10/105 COULD BE RELATED TO THE ISSUE WITH SENSOR. 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 TABLE DURING PROCEDURE, WAS TO REOCCUR.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19402906 ↗
• MalfunctionMar 20, 2024Circuit Failure; Unintended Movement; Circuit Failure; Unintended Movement

  ON 22ND FEBRUARY 2024, GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR TABLETOPS - 118010A0 - BASIS TABLETOP, INDIVIDUAL CONFIGURATION USED WITH 118001C0 - MAGNUS TABLE COLUMN, MOBILE. AS STATED, THE OPERATING TABLE SUDDENLY COULD NO LONGER BE OPERATED CORRECTLY DURING THE PROCEDURE. THE OPERATING TABLE MOVED IN THE OPPOSITE DIRECTION THAN INDICATED (DESIRED MOVEMENT: TABLE UP, TILTING TO THE RIGHT; ACTUAL MOVEMENT: TABLE DOWN, TILTING TO THE LEFT). ACCORDING TO THE CUSTOMER'S ALLEGATION, THE PATIENT COULD HAVE INADVERTENTLY INJURED IMPORTANT ORGANS AND STRUCTURES (NERVES/VESSELS) WITH THE SURGICAL INSTRUMENTS DURING LAPAROSCOPY OR FALLEN FROM THE OPERATING TABLE. THERE WAS NO INJURY REPORTED, HOWEVER, WE DECIDED TO REPORT THE ISSUE BASED ON THE POTENTIAL FOR SERIOUS INJURY IF THE SITUATION, NAMELY THE UNINTENDED MOVEMENT OF THE TABLETOP DURING THE PROCEDURE, WAS TO REOCCUR.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18941433 ↗
• MalfunctionFeb 2, 2024Positioning Failure; Failure to Interrogate; Electrical Overstress; Positioning Failure; Failure to Interrogate; Electrical Overstress

  ON 22ND JANUARY 2024 GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR TABLE TOPS - 118010A0 - BASIS TABLE TOP,INDIVIDUAL CONFIGURATION. AS IT WAS STATED, ERROR 107 (OVERCURRENT DETECTED) WAS DISPLAYED DURING STOMA PROCEDURE AND THE ANESTHETIZED PATIENT HAD TO BE TRANSFERRED INTO ANOTHER OPERATING ROOM. THE ISSUE RESULTED IN A 1-HOUR DELAY. 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 18630385 ↗
• MalfunctionJan 31, 2024Positioning Failure; Misconnection; Unintended Movement; Positioning Failure; Misconnection; Unintended Movement

  ON 17TH JANUARY 2024 GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR TABLETOPS - 118010A0 - BASIS TABLETOP, INDIVIDUAL CONFIGURATION USED WITH 118001C0 - MAGNUS TABLE COLUMN, MOBILE. THE RECEIVED CUSTOMER ALLEGATION REGARDED A NON-REPORTABLE ISSUE. ON 26TH JANUARY 2024, ADDITIONAL INFORMATION WAS RECEIVED. AS IT WAS STATED, THE UNINTENDED MOVEMENT OF THE TABLETOP OCCURRED DURING THE INTRAOPERATIVE PHASE OF LAPAROSCOPIC DIAGNOSTICS AND POSSIBLE HERNIA REPAIR WITH MESH INSERT ON THE ANESTHETIZED PATIENT. THE INCISION HAD ALREADY BEEN MADE AT THE TIME OF INCIDENT. THE OPERATING TABLE MOVED IN THE OPPOSITE DIRECTION THAN INDICATED (DESIRED MOVEMENT: TRENDELENBURG POSITION, TILTING TO THE RIGHT; ACTUAL MOVEMENT: ANTI-TRENDELENBURG POSITION, TILTING TO THE LEFT). FOLLOWING THE UNINTENDED MOTION, THE BUTTONS ON THE REMOTE CONTROL DID NOT WORK AND THE TABLETOP COULD NOT BE MOVED FOR 30 MINUTES WHICH MADE THE DIAGNOSIS EXTREMELY DIFFICULT FOR THE SURGEON. THE OPERATION COULD NOT BE COMPLETED AND WAS ENDED EARLY. THE PATIENT HAD TO REMAIN UNDER ANESTHESIA FOR 10 MORE MINUTES AS THE TABLE STILL COULD NOT BE MOVED. AFTER THAT TIME, THE TABLE WORKED AGAIN AND THE ANESTHESIA COULD BE ENDED. ACC

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18612822 ↗
• MalfunctionDec 28, 2023Failure to Sense; Failure to Align; Failure to Sense; Failure to Align

  ON 15TH DECEMBER 2023 GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR TABLE TOPS - 118010A0 - BASIS TABLE TOP,INDIVIDUAL CONFIGURATION. AS IT WAS STATED, ERROR 112 (THE LEFT AND RIGHT SEGMENTS HAVE AN INADMISSIBLE POSITION DIFFERENCE) ON SEGMENT 10 WAS DISPLAYED DURING A TREATMENT ON THE ANESTHETIZED PATIENT. THE ERROR RESOLVED BY ITSELF, HOWEVER, THE ISSUE LED TO A DELAY OF APPROXIMATELY 2 MINUTES. ACCORDING TO THE INITIAL EVALUATION, NO ERRORS WERE FOUND DURING THE INSPECTION. 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 18408185 ↗