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Vividimage 4K RLM274KRecalls & reported problems

Black Diamond Video, Inc. · The Vividimage 27-inch 4K Surgical Monitor 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

Adverse event reports
12
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 12 adverse event reports that list this exact device (DI 00724995195175), received between Jan 5, 2026 and Jun 17, 2026 — classified as 12 malfunctions.

The most frequently reported specific device problem is “Display or Visual Feedback Problem” (10 reports).

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

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 3 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 9 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520269
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Display or Visual Feedback Problem10
  • Erratic or Intermittent Display2

Patient problems

  • No Clinical Signs, Symptoms or Conditions12

Recent adverse event reports

The 12 most recent of 12 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJun 17, 2026Display or Visual Feedback Problem

    THE USER FACILITY REPORTED THAT THE SETTINGS ON THE LIGHTING SYSTEM CONNECTED TO THEIR HEXAVUE CUSTOM ROOM RACK ARE CHANGING. NO REPORT OF PATIENT/PROCEDURE INVOLVEMENT. NO REPORT OF INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25532621 ↗
  • MalfunctionJun 17, 2026Display or Visual Feedback Problem

    THE USER FACILITY REPORTED THAT PRIOR TO A PATIENT PROCEDURE THEIR VIVIDIMAGE 4K SURGICAL DISPLAY WAS NOT RESPONDING AND SHOWING DISTORTED IMAGES. NO REPORT OF INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25532610 ↗
  • MalfunctionJun 17, 2026Display or Visual Feedback Problem

    THE USER FACILITY REPORTED THAT PRIOR TO A PATIENT PROCEDURE THEIR VIVIDIMAGE 4K SURGICAL DISPLAY WAS NOT RESPONDING AND SHOWING DISTORTED IMAGES. NO REPORT OF INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25532595 ↗
  • MalfunctionJun 16, 2026Display or Visual Feedback Problem

    THE USER FACILITY REPORTED THAT THEIR VIVIDIMAGE SURGICAL MONITOR WAS "INTERMITTENTLY GOING BLANK". NO REPORT OF INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25524340 ↗
  • MalfunctionJun 15, 2026Display or Visual Feedback Problem

    THE USER FACILITY REPORTED THAT THE MONITOR CONNECTED TO THEIR VIVIDIMAGE 4K SURGICAL DISPLAY HAS NO VIDEO AND "ARTIFACTS" DISPLAYING ON THE SCREEN. NO REPORT OF INJURY OR PROCEDURE DELAY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25513545 ↗
  • MalfunctionJun 15, 2026Display or Visual Feedback Problem

    THE USER FACILITY REPORTED THAT THEIR VIVIDIMAGE 4K SURGICAL DISPLAYS WERE SHOWING DISTORTED DISPLAYS. NO REPORT OF INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25509641 ↗
  • MalfunctionJun 15, 2026Display or Visual Feedback Problem

    THE USER FACILITY REPORTED THAT THEIR VIVIDIMAGE 4K SURGICAL DISPLAYS WERE SHOWING DISTORTED DISPLAYS AND HAD INTERMITTENT POWER ISSUES. NO REPORT OF INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25509136 ↗
  • MalfunctionJun 15, 2026Display or Visual Feedback Problem

    THE USER FACILITY REPORTED THAT THEIR VIVIDIMAGE 4K SURGICAL DISPLAYS WERE SHOWING DISTORTED DISPLAYS. NO REPORT OF INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25508704 ↗
  • MalfunctionJun 15, 2026Display or Visual Feedback Problem

    THE USER FACILITY REPORTED THAT PRIOR TO A PATIENT PROCEDURE THEIR VIVIDIMAGE 4K SURGICAL DISPLAY WENT BLACK. NO REPORT OF INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25507483 ↗
  • MalfunctionJan 6, 2026Display or Visual Feedback Problem

    THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE THE VIVID IMAGE 4K SURGICAL DISPLAY SWITCHED FROM HAVING A CLEAR IMAGE TO A "DISTORTED IMAGE WITH VERTICAL LINES." ANOTHER MONITOR WAS UTILIZED TO COMPLETE THE PATIENT PROCEDURE. THE PROCEDURE WAS COMPLETED SUCCESSFULLY. NO REPORT OF INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23973561 ↗
  • MalfunctionJan 5, 2026Erratic or Intermittent Display

    THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE THE IMAGE WAS FLICKERING ON THEIR VIVIDIMAGE 4K SURGICAL MONITOR. THE PROCEDURE WAS COMPLETED SUCCESSFULLY USING A SECOND MONITOR WITH NO REPORT OF INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23967571 ↗
  • MalfunctionJan 5, 2026Erratic or Intermittent Display

    THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE THE IMAGE TO THEIR VIVIDIMAGE 4K SURGICAL MONITOR LOSES FOCUS AND INTERMITTENTLY DISPLAYS BLACK LINES. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH NO REPORT OF INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23966587 ↗

Other CAMERA, SURGICAL AND ACCESSORIES devices

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.