Vividimage 4K RLM314K3NPWRRecalls & reported problems
Black Diamond Video, Inc. · The Vividimage 31-inch 4K Surgical Display is designed for the most demanding surgical environments through its delivery of realistic color accuracy, improved visualization of fine structure details, and enhanced depth perception. · Class 1
All models of Vividimage 4K (4)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00724995195137), received between Mar 19, 2026 and Jun 25, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Display or Visual Feedback Problem” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Display or Visual Feedback Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 25, 2026Adverse Event Without Identified Device or Use Problem
THE USER FACILITY REPORTED THE MONITOR TO THEIR VIVIDIMAGE 4K SURGICAL DISPLAY WAS "FLICKERING" DURING A PATIENT PROCEDURE. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITHOUT DELAY. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25626922 ↗MalfunctionMar 19, 2026Display or Visual Feedback Problem
THE USER FACILITY REPORTED THAT BLACK LINES WERE DISPLAYED ON THEIR VIVIDIMAGE 4K MONITOR. NO REPORT OF PROCEDURE DELAY OR INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24643201 ↗
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
- VidiaPort 4028110Baxter Medical Systems GmbH + Co. KG · CAMERA, SURGICAL AND ACCESSORIES1 recall1 report
- Vividimage 4K RLM314K3Black Diamond Video, Inc. · CAMERA, SURGICAL AND ACCESSORIES51 reports
- BARCO MDSC-8527Barco NV · 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 and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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