Barco MDSC-8255Recalls & reported problems
Barco NV · MDSC-8255 LED · Class 1
- 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 05415334031838), received between Oct 18, 2024 and Oct 18, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “No Display/Image” (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.
Reports received per month
Most reported problems
Device problems
- No Display/Image1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 18, 2024No Display/Image; No Display/Image
DURING THE ANGIOGRAPHY IN CATH LAB MONITOR WAS SUDDENLY GET OFF AND NOT WORKING AFTER THAT. OTHER OPTION DURING ANGIOGRAPHY PROCEDURE AS THERE WAS NO OTHER MONITOR SO PATIENT WENT INTO CRITICAL STAGE, PATIENT WAS TRANSFERRED TO ANOTHER HOSPITAL AND THE PATIENT WAS COVERED IN THE TREATMENT PANEL.
Patient problems: Insufficient Information
MAUDE report 20481757 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.