Barco MDSC-8232 (REF K9352051)Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 05415334001367), received between Jul 15, 2024 and Oct 22, 2024 — classified as 2 malfunctions.

The most frequently reported specific device problem is “No Display/Image” (2 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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionOct 22, 2024No Display/Image; No Display/Image

  3 MONITORS WERE DROPPING IMAGE OR SIGNAL DURING TURP PROCEDURE.

  Patient problems: Insufficient Information

  MAUDE report 20503292 ↗
• MalfunctionJul 15, 2024No Display/Image; Electromagnetic Interference; No Display/Image; Electromagnetic Interference

  WE WERE INFORMED ABOUT A HOSPITAL EXPERIENCING 2 ISSUES. WITH BOTH OF OLYMPUS TOWERS GOING DOWN TODAY IT IS AFFECTING SERVICE DELIVERY OF UROLOGY. THE HOSPITAL'S UROCAMS AND URETEROSCOPES ONLY FIT INTO THIS TOWER (AND ON PENDANT IN OR5 IF ORTHOPAEDICS IS NOT OCCUPYING THE ROOM) RECENTLY THE CABLE WAS CHANGED, HOWEVER INTERMITTENTLY IT HAS TURNED OFF MID PROCEDURE. THE STANDBY LIGHT ALTERNATES FROM RED TO GREEN AND NOW THE MONITOR WILL NOT TURN ON AT ALL. THE PATIENT WAS NOT AFFECTED. THERE WAS DIATHERMY USED DURING THE CASE. THE LEADS WERE SEPARATED TO MINIMISE INTERFERENCE. THE UNIT WAS NOT DISCONNECTED FOR 5 MINS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19738619 ↗