FDA Adverse Event Malfunction Summary report: N

BLACKDIAMOND HDMI CABLE

MDR report key: 19981304 · Received August 14, 2024

Report

Report Number
3008776287-2024-00014
Event Type
Malfunction
Date Received
August 14, 2024
Date of Event
April 5, 2024
Report Date
August 14, 2024
Manufacturer
BLACK DIAMOND VIDEO, INC.
Product Code
KQM
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

THE REPORT DID NOT IDENTIFY THE NAME OR LOCATION OF THE USER FACILITY OF THE DEVICE IN QUESTION THEREFORE, ADDITIONAL INFORMATION COULD NOT BE OBTAINED. TO DATE WE HAVE NOT BEEN INFORMED OF THIS EVENT DIRECTLY FROM THE USER FACILITY. A FOLLOW-UP REPORT WILL BE SUBMITTED SHOULD ADDITIONAL INFORMATION BECOME AVAILABLE. NO ADDITIONAL ISSUES HAVE BEEN REPORTED.

Description of Event or Problem · 0

THE USER FACILITY REPORTED VIA MEDWATCH REPORT MW5156331 THAT SMOKE WAS EMITTING FROM THEIR BLACK DIAMOND HDMI CABLE. NO REPORT OF INJURY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
234798 BLACKDIAMOND HDMI CABLE CAMERA, SURGICAL AND ACCESSORIES KQM BLACK DIAMOND VIDEO, INC.

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown