FDA Adverse Event Malfunction Summary report: N

X7000 XENON LIGHTSOURCE

MDR report key: 2210187 · Received May 16, 2011

Report

Report Number
2936485-2011-00326
Event Type
Malfunction
Date Received
May 16, 2011
Date of Event
April 26, 2011
Report Date
April 26, 2011
Manufacturer
STRYKER ENDOSCOPY SAN JOSE
Product Code
FCW
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

ADDITIONAL INFO WILL BE PROVIDED ONCE THE INVESTIGATION HAS BEEN COMPLETED.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE UNIT IS OVER HEATING AND TURNING OFF.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 X7000 XENON LIGHTSOURCE LIGHTSOURCE FCW STRYKER ENDOSCOPY SAN JOSE

Patients

Seq Age Sex Outcome Treatment
1 UNK