BARCO MDSC-8532 (REF K9352402B)Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05415334042674), received between Jul 16, 2025 and Jul 16, 2025 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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.

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.

• MalfunctionJul 16, 2025Detachment of Device or Device Component; Detachment of Device or Device Component

  ON JUNE 23, WE RECEIVED A COMPLAINT FROM A CUSTOMER ABOUT A FRONT FILTER DETACHMENT. AFTER THE WEEKEND, THE CUSTOMER ENTERED THEIR DEMO ROOM AND NOTICED THAT THE FRONT FILTER (GLASS) HAD COMPLETELY DETACHED FROM THE DISPLAY, FALLEN DOWN AND SHATTERED INTO PIECES. THERE WAS NOBODY NEAR THE DISPLAY AT THE TIME THE GLASS HAD FALLEN. NOBODY HAS SEEN THE GLASS FALLING DOWN. NO INJURIES HAVE BEEN REPORTED. ONE WEEK EARLIER, THE SAME CUSTOMER HAD INFORMED US THAT THE FRONT GLASS OF THE SAME DISPLAY IN THE DEMO ROOM HAD PARTLY DETACHED. IT WAS STILL PARTIALLY ATTACHED TO THE DISPLAY AND WAS NOT COMPLETELY LOOSE. INSTEAD OF TAKING THE DISPLAY OUT OF SERVICE, AS INSTRUCTED IN THE INSTRUCTIONS FOR USE, THE USER PUSHED BACK THE FRONT GLASS. THE EVENT OF PARTIAL DETACHMENT HAS NO RISK AT ALL THAT IT COULD CAUSE OR CONTRIBUTE TO ANY HARM WHATSOEVER, IF IT WOULD OCCUR AGAIN.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22519606 ↗