Barco MDSC-8232 (REF K9352051B)Recalls & reported problems
Barco NV · MDSC-8231 12G · Class 1
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05415334026568), received between Mar 27, 2024 and Mar 27, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Electromagnetic Interference” (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
- Electromagnetic Interference1
- No Display/Image1
Patient problems
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 27, 2024No Display/Image; Electromagnetic Interference; No Display/Image; Electromagnetic Interference
DR ADVISED THAT HE HAD A PATIENT SUFFER TUR SYNDROME DURING A TURBT (RESECTION OF BLADDER TUMOUR) AS A RESULT OF LOSING VISION WITH THE BARCO MONITOR. DR NEEDED TO REVERT BACK TO THE OLD STACK WHICH ADDED TIME TO THE PROCEDURE. THE PROCEDURE TOOK LONGER THAN INTENDED AS A RESULT OF THE EQUIPMENT ISSUE, AND THEREFORE THE PATIENT SUFFERED TUR SYNDROME.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 18986191 ↗
Other Camera, Surgical And Accessories devices
- HexaVue HexaVue SCC 1.0Black Diamond Video, Inc. · CAMERA, SURGICAL AND ACCESSORIES245 reports
- HexaVue HexaVue IPBlack Diamond Video, Inc. · CAMERA, SURGICAL AND ACCESSORIES80 reports
- Maquet Orchide ARD569204944Maquet Sas · Camera, Surgical And Accessories1 recall2 reports
- BARCO MDSC-8527Barco NV · Camera, Surgical And Accessories1 recall1 report
- Vividimage 4K RLM314K3Black Diamond Video, Inc. · CAMERA, SURGICAL AND ACCESSORIES51 reports
- VidiaPort 4028110Baxter Medical Systems GmbH + Co. KG · CAMERA, SURGICAL AND ACCESSORIES1 recall1 report
- Maquet Orchide ARD568803967Maquet Sas · Camera, Surgical And Accessories1 recall0 reports
- AESCULAP JG910Aesculap AG · CAMERA, SURGICAL AND ACCESSORIES1 recall0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.