BARCO MDSC-8527Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05415334043312), received between Mar 27, 2024 and Mar 27, 2024 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (1 report).

1 FDA recall record name this device's identifier, 1 still open.

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.

Recalls naming this device

1. Dec 20, 2023Open, Classified

   Barco became aware of a problem with I2C cables in the manufacturing process of a limited batch of MDSC-85xx NXF products. The functionality of the built-in MNA decoder is blocked.

   Z-0979-2024 · Root cause: Under Investigation by firm · FDA record ↗

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.

• MalfunctionMar 27, 2024Detachment of Device or Device Component; Device Handling Problem; Detachment of Device or Device Component; Device Handling Problem

  COVER FOR CABLE CONNECTIONS (PLASTIC COVER) FELL WHEN MOVING THE MONITOR ON THE OPERATING TABLE DURING SURGICAL PREPARATION. OPERATING TABLE UNSTERILE LONGER OPERATION AND ANESTHESIA TIME FOR THE PATIENT. COVER PROBABLY CAME LOOSE DURING CLEANING.

  Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions

  MAUDE report 18985050 ↗