MAUDE Adverse Event Report: Black Diamond Video, Inc. Vividimage 4K; Surgical Display

Model Number	RLM314K3
Medical Device Problem Code	Display or Visual Feedback Problem (1184)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	07/30/2026
Type of Reportable Event	Malfunction
Event or Problem Description
The user facility reported an intermittent ¿blinky¿ image on their vividimage 4k surgical display during a patient procedure.The procedure was completed successfully with a different display in the room.No report of injury or procedure delay.
Additional Manufacturer Narrative
A steris service technician arrived onsite to inspect the vividimage 4k surgical display and was unable to duplicate the reported event.The technician found that the fiber optic cable was pinched which likely caused the reported event.To resolve the issue the technician repositioned the fiber cable, tested the function and operation of the unit, confirmed it to be operating to specification, and returned the unit to service.The unit was installed in 2024 and is not under steris service agreement for preventive maintenance activities; the user facility is responsible for all maintenance activities.No additional issues have been reported.

• Brand Name: Vividimage 4K
• Common Device Name: Surgical Display
• 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 ; +1(440)259-7401
• MDR Report Key: 50485258
• Report Number: 3008776287-2026-00605
• Device Sequence Number: 10112191
• Product Code: KQM
• UDI-Device Identifier: 00724995195113
• UDI-Public: (01)00724995195113(11)240701
• Combination Product (Y/N): N
• Initial Reporter State: IL
• 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): 08/27/2026

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: RLM314K3
• Device Catalogue Number: RLM314K3
• 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: 07/30/2026
• Initial Report FDA Received Date: 08/27/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 07/01/2024
• 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