MAGNUS T285.7000Recalls & reported problems
MAQUET GmbH · MAGNUS Carbon-fibre table top · Class 2
Data updated Oct 16, 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 04046768067165), received between Jun 18, 2024 and Jun 18, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Battery Problem” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Battery Problem1
- Circuit Failure1
- Failure to Sense1
- Loose or Intermittent Connection1
- Power 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.
MalfunctionJun 18, 2024Circuit Failure; Loose or Intermittent Connection; Failure to Sense; Battery Problem; Power Problem; Circuit Failure; Loose or Intermittent Connection; Failure to Sense; Battery Problem; Power Problem
ON 30TH MAY 2024, GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR COLUMNS - 118001B1 - HYBRID OR TABLE COLUMN, SURFACE-MOUNTED. AS IT WAS STATED, ERROR 174 (POSITION ERROR) OCCURRED WHILE MOVING THE TABLE DURING TRANSCATHETER AORTIC VALVE REPAIR ON THE ANESTHETIZED PATIENT UNDER INTRAVENOUS MODERATE SEDATION. THE STAFF WAITED FOR ALMOST AN HOUR WHILE TROUBLESHOOTING WAS DONE BEFORE THE SURGEON DECIDED TO ABORT THE CASE. THE PATIENT WAS TAKEN TO THE RECOVERY ROOM. BASED ON INFORMATION PROVIDED BY THE TECHNICIAN FOLLOWING SERVICE VISIT ON SITE, THE TABLE WAS MOVING CORRECTLY AND COMMUNICATING WITH PHILIPS SYSTEM AFTER RECALIBRATION AND RESET OF THE TABLE AND IMAGINING DEVICE. ACCORDING TO THE CUSTOMER, THE BATTERIES IN THE SYSTEM UPS HAD JUST BEEN CHANGED WHICH COULD HAVE CAUSED A POWER GLITCH THAT INTERRUPTED COMMUNICATION AND CAUSED A LOSS OF CALIBRATION DATA. 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 LEADING TO RESCHEDULING OF THE PROCEDURE, WAS TO REOCCUR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19555986 ↗
Other Table, Radiologic devices
- ORT300 TableIMRIS Imaging, Inc. · Table, Radiologic2 recalls6 reports
- NA 6265300GE Medical Systems, L.L.C. · Table, radiologic2 recalls0 reports
- PST500 4080300Baxter Medical Systems GmbH + Co. KG · Table, radiologic1 recall4 reports
- TS 7500 1730720Baxter Medical Systems GmbH + Co. KG · Table, radiologic1 recall1 report
- TS 7500 1730731Baxter Medical Systems GmbH + Co. KG · Table, radiologic1 recall0 reports
- TS 7500 1717020Baxter Medical Systems GmbH + Co. KG · Table, radiologic1 recall0 reports
- TS 7500 1730732Baxter Medical Systems GmbH + Co. KG · Table, radiologic1 recall0 reports
- NA 7265300Ge Healthcare(Tianjin) Company Limited · Table, radiologic1 recall0 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 14, 2026 · each report above links to its original FDA record
- 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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