MAUDE Adverse Event Report: BLACK DIAMOND VIDEO, INC. VIVIDIMAGE 4K; MONITOR

Model Number	RLM314K3NPWR
Medical Device Problem Code	Display or Visual Feedback Problem (1184)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	02/17/2026
Type of Reportable Event	Malfunction
Event or Problem Description
The user facility reported that black lines were displayed on their vividimage 4k monitor.No report of procedure delay or injury.
Additional Manufacturer Narrative
A steris service technician arrived onsite following the reported event and found that the video router required resetting.The technician reset the video router, confirmed the vividimage 4k monitor to be operating to specifications and returned the devices to service.No additional issues have been reported.

• Brand Name: VIVIDIMAGE 4K
• Common Device Name: MONITOR
• Manufacturer (Section D): BLACK DIAMOND VIDEO, INC.; 503 canal blvd.; richmond CA 94804
• Manufacturer (Section G): BLACK DIAMOND VIDEO, INC.; 503 canal blvd.; richmond CA 94804
• Manufacturer Contact: daniel davy ; 5960 heisley road; mentor, OH 44060 ; 4402597401
• MDR Report Key: 24643201
• Report Number: 3008776287-2026-00074
• Device Sequence Number: 9906349
• Product Code: KQM
• UDI-Device Identifier: 00724995195137
• UDI-Public: (01)00724995195137(11)210921
• Combination Product (Y/N): N
• Initial Reporter State: FL
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: User Facility
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 03/19/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: RLM314K3NPWR
• Device Catalogue Number: RLM314K3NPWR
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 02/17/2026
• Initial Report FDA Received Date: 03/19/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Reuse
• Patient Sequence Number: 1
• Patient Sex: Unknown