MAGNUS carbon fibre table top 118016A5Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04046768040779), received between Aug 2, 2023 and Aug 2, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Communication or Transmission 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 18, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 2, 2023Communication or Transmission Problem; Device Sensing Problem; Positioning Problem; Communication or Transmission Problem; Device Sensing Problem; Positioning Problem

  ON (B)(6) 2023 GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR COLUMNS ¿ 118001B1 - HYBRID OR TABLE COLUMN, SURFACE-MOUNTED. AS IT WAS STATED, THE COMMUNICATION ISSUES OCCURRED BETWEEN THE HYBRID OR TABLE COLUMN AND PHILIPS ANGIOGRAPHY DEVICE DURING IMAGINING. THE TABLE STOPPED MOVING TOWARDS THE HEAD SIDE. ACCORDING TO THE PROVIDED INFORMATION, FOLLOWING THE EVENT, THE ANGIOGRAPHY DEVICE WAS RESTARTED AND THE PROCEDURE WAS SUCCESSFULLY PERFORMED WITHOUT INTERLOCKING WITH THE GETINGE REMOTE CONTROL. THE ISSUE LED TO A DELAY OF APPROXIMATELY 5 MINUTES. THERE WAS NO INJURY REPORTED, HOWEVER, WE DECIDED TO REPORT THE ISSUE BASED ON THE POTENTIAL FOR SERIOUS INJURY IF THE SITUATION, NAMELY A DELAY IN SURGERY RESULTING IN PROLONGED ANESTHESIA TIME, WAS TO REOCCUR.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17447237 ↗