NA IDSS-SCCRecalls & reported problems
Black Diamond Video, Inc. · The IDSS Integration System with Surgical Camera Control is an integrated audio-visual system which combines monitors, medical imaging devices, lights, music, and cameras. · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 15
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 15 adverse event reports that list this exact device (DI 00724995198473), received between Jul 29, 2026 and Sep 28, 2026 — classified as 1 injury, 14 malfunctions.
The most frequently reported specific device problem is “Display or Visual Feedback Problem” (15 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
Most reported problems
Device problems
- Display or Visual Feedback Problem15
- Erratic or Intermittent Display1
Patient problems
- No Clinical Signs, Symptoms or Conditions15
Recent adverse event reports
The 15 most recent of 15 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 28, 2026Display or Visual Feedback Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50923785 ↗MalfunctionSep 28, 2026Display or Visual Feedback Problem
The user facility reported that the monitors to their BDV IDSS Custom Room Rack are flickering. This event did not occur during a patient procedure. No report of injury.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50917792 ↗MalfunctionSep 28, 2026Display or Visual Feedback Problem
The user facility reported that the touch panel to their BDV IDSS Custom Room Rack was displaying a distorted preview image. This event did not occur during a patient procedure. No report of injury.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50916599 ↗MalfunctionSep 28, 2026Display or Visual Feedback Problem
The user facility reported that the monitors to their BDV IDSS Custom Room Rack have lost signal and were not displaying images. This event did not occur during a patient procedure. No report of injury.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50916160 ↗MalfunctionSep 25, 2026Display or Visual Feedback Problem
The user facility reported that during a patient procedure the monitor to their BDV IDSS Custom Room Rack was experiencing image instability and screen flickering. No report of procedure delay. No report of injury.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50900177 ↗MalfunctionSep 24, 2026Display or Visual Feedback Problem
The user facility reported the monitor to their BDV IDSS Custom Room Rack was flickering and ¿making a buzzing sound¿. No report of procedure involvement. No report of injury.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50876760 ↗MalfunctionSep 24, 2026Display or Visual Feedback Problem
The user facility reported the monitor to their BDV IDSS Custom Room Rack was experiencing ¿no video¿ and ¿intermittent freezing¿. No report of procedure involvement. No report of injury.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50876683 ↗MalfunctionSep 23, 2026Display or Visual Feedback Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50869343 ↗MalfunctionSep 23, 2026Display or Visual Feedback Problem
The user facility reported that the touch panel to their BDV IDSS Custom Room Rack was displaying a distorted preview image. This event did not occur during a patient procedure. No report of injury.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50869311 ↗MalfunctionSep 23, 2026Display or Visual Feedback Problem
The user facility reported that the monitors to their BDV IDSS Custom Room Rack were displaying black boxes on the image. This event did not occur during a patient procedure. No report of injury.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50869306 ↗MalfunctionSep 17, 2026Display or Visual Feedback Problem
The user facility reported the display to the touch panel used with the BDV IDSS Custom Room Rack had a distorted image. The event did not occur during a patient procedure. No report of injury.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50808088 ↗MalfunctionAug 27, 2026Display or Visual Feedback Problem
The user facility reported that the touch panel used with the BDV IDSS Custom Room Rack had a distorted image. No report of procedure involvement. No report of injury.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50482868 ↗MalfunctionAug 27, 2026Display or Visual Feedback Problem
The user facility reported that the surgical displays to their BDV IDSS Custom Room Rack were flashing and the wall monitors were not showing images. This event did not occur during a patient procedure. No report of injury.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50480091 ↗MalfunctionAug 26, 2026Erratic or Intermittent Display; Display or Visual Feedback Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50457663 ↗InjuryJul 29, 2026Display or Visual Feedback Problem
The user facility reported that the monitors to their BDV IDSS Custom Room Rack intermittently go black and reboot. This event did not occur during a patient procedure. No report of injury.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50069516 ↗
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- 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 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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