Stationary transformer unit 115080A0Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 04046768080195), received between Dec 22, 2023 and Jan 27, 2026 — classified as 3 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionJan 27, 2026Positioning Failure

  GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR DEVICES 115080A0 - STATIONARY TRANSFORMER USED WITH 118001B2 - HYBRID OR TABLE COLUMN, SURFACE-MOUNTED. ACCORDING TO THE USER STATEMENT, THE OR TABLE FAILED TO MOVE DURING THE PROCEDURE. NEITHER THE REMOTE CONTROL NOR THE CONTROL PANEL COULD OPERATE IT DURING A NEUROSURGICAL ANGIOGRAPHY 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 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 24187547 ↗
• MalfunctionFeb 3, 2025Positioning Failure; Battery Problem; Positioning Failure; Battery Problem

  GETINGE BECAME AWARE OF AN INCIDENT INVOLVING ONE OF OUR ACCESSORIES ¿ THE 115080A0 STATIONARY TRANSFORMER, USED WITH THE 115002A0 - ALPHAMAQUET OPERATING TABLE COLUMN. AS IT WAS STATED, THE OPERATING TABLE EXPERIENCED A COMPLETE BLOCKAGE. THE CUSTOMER ALLEGED THAT THE REMOTE CONTROL WAS NOT FUNCTIONING PROPERLY. BASED ON INFORMATION PROVIDED BY THE BIOMEDICAL TECHNICIAN, THE ISSUE WAS LINKED TO A PROBLEM WITH THE BACKUP BATTERIES. FURTHER DETAILS REGARDING THE INCIDENT WERE REQUESTED. LATER ON, IT WAS CONFIRMED THAT THE MALFUNCTION RESULTED IN THE INABILITY TO CONTINUE THE OPERATION, REQUIRING THE SURGERY TO BE POSTPONED. 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 PATIENT AS REQUIRED RESULTING IN RESCHEDULING OF THE SURGERY, WAS TO REOCCUR.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21291040 ↗
• MalfunctionDec 22, 2023Positioning Failure; Charging Problem; Positioning Failure; Charging Problem

  ON 10TH DECEMBER 2023 GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR ACCESSORIES - 115080A0 - STATIONARY TRANSFORMER USED WITH 118001B1 - HYBRID OR TABLE COLUMN, SURFACE-MOUNTED. AS IT WAS STATED, DURING THE SURGERY ON THE ANESTHETIZED PATIENT, AN ALARM SOUND APPEARED AS SOON AS THE USER PRESSED BUTTON ON THE REMOTE CONTROL. THE INTERFACE DISPLAYED THAT THE MOVEMENT IS BEING INITIALISED, HOWEVER, THE TABLE DID NOT MOVE. FOLLOWING THE SERVICE VISIT ON SITE, THE TECHNICIAN STATED THAT THE TABLE COULD NOT BE MOVED WITH REMOTE CONTROL NOR OVERRIDE PANEL DUE TO AN ABNORMAL OUTPUT VOLTAGE RELATED TO A FAULTY CHARGING VOLTAGE REGULATOR. 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 DURING SURGERY DUE TO ISSUE WITH A CHARGING VOLTAGE REGULATOR, WAS TO REOCCUR.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18388800 ↗