Barco MDSC-8232 (REF K9307927)Recalls & reported problems
Barco NV · MDSC-8231 MNA · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- 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 05415334001817), received between Nov 10, 2025 and Nov 10, 2025 — 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
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 10, 2025No Display/Image; No Display/Image
THE DISPLAY WENT BLANK TWICE DURING A TURP PROCEDURE. THE STAFF WAS UNABLE TO REBOOT IT. THERE WAS ANOTHER SCREEN AVAILABLE ON A DIFFERENT STACK. THE PROCEDURE WAS EXTENDED BECAUSE OF THE ISSUE AND WAS COMPLETED USING THE SCREEN ON THE OTHER STACK.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23509387 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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