Transfer table top 118013A0Recalls & reported problems
MAQUET GmbH · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04046768040731), received between Mar 15, 2024 and Mar 15, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (1 report).
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
Most reported problems
Device problems
- Break1
- Positioning Failure1
- Use of Device Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 15, 2024Break; Positioning Failure; Use of Device Problem; Break; Positioning Failure; Use of Device Problem
ON 1ST MARCH 2024, GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR DEVICES - TABLE TOP USED WITH 118001D0 - MAGNUS OR-TABLE COLUMN, INDEPENDENTLY MANOEUVRABLE. AS IT WAS STATED, AN ANESTHETIZED PATIENT IN HEAD PINS FOR A NEUROSURGICAL PROCEDURE WAS ON THE MAGNUS TABLE TOP WHICH WAS LOCATED ON MRI TRANSFER TABLE (MANUFACTURED BY GE). THE TABLE TOP WAS NOT ABLE TO BE TRANSFERRED FROM THE GE TRANSFER TABLE TO THE MAGNUS COLUMN. THE STAFF TRIED TO ENGAGE SLIDE MECHANISM FOR APPROXIMATELY 25-30 MINUTES, HOWEVER, THEY WERE UNSUCCESSFUL. CONSEQUENTLY, IT WAS DECIDED TO PHYSICALLY TRANSFER THE PATIENT OUT OF THE HEAD PINS AND OFF THE GE MRI TRANSFER TABLE AND PLACE THEM ONTO THE NONE MRI MAGNUS TABLE TOP. THIS RESULTED IN A DELAY OF APPROXIMATELY 45 MINUTES. ACCORDING TO PROVIDED INFORMATION, THE PATIENT DID NOT SUFFER ANY HARM DUE TO THE ISSUE. GE HAVE ATTENDED THE TRUST TO SERVICE AND REPAIR THE MRI TRANSFER TABLE AND SUGGESTED A RECALIBRATION OF THEIR TABLE ALONGSIDE THE MAGNUS TABLE TOP. FOLLOWING THE SERVICE VISIT ON SITE PERFORMED BY GETINGE, THE ACTUATOR LOCKING PIN WAS FOUND TO BE SNAPPED. THE PIN NOT ENGAGING WITH TROLLEY RESULTED IN NOT BEING ABLE TO RELEASE TRANSFER BOARD. THE
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18911563 ↗
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- 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 and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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