MAUDE Adverse Event Report: BLACK DIAMOND VIDEO, INC. VIVIDIMAGE D HD; SURGICAL DISPLAY

Model Number	RLM27HD3
Medical Device Problem Code	Display or Visual Feedback Problem (1184)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	06/03/2024
Type of Reportable Event	Malfunction
Event or Problem Description
The user facility reported that during patient procedures the monitors to their vividimage surgical display were flickering.The procedures were completed successfully following short delays.No report of injury.
Additional Manufacturer Narrative
A steris service technician arrived onsite following the reported event to inspect the unit and found that user facility personnel had altered the power cabling, subsequently causing the reported event.To resolve the issue, the technician repaired the power cabling.The unit was tested, confirmed to be operating according to specification, and returned to service.While onsite the technician counseled user facility personnel on the proper handling of the power cabling.No additional issues have been reported.

• Brand Name: VIVIDIMAGE D HD
• 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 ; 4402597401
• MDR Report Key: 25408961
• Report Number: 3008776287-2026-00188
• Device Sequence Number: 10311670
• Product Code: KQM
• UDI-Device Identifier: 00724995195069
• UDI-Public: (01)00724995195069(11)230503
• Combination Product (Y/N): N
• Initial Reporter State: MA
• 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): 06/05/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Model Number: RLM27HD3
• Device Catalogue Number: RLM27HD3
• 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: 06/03/2024
• Initial Report FDA Received Date: 06/05/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 05/03/2023
• 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