FDA Adverse Event Malfunction Summary report: N

X7000 XENON LIGHTSOURCE

MDR report key: 2082046 · Received April 26, 2011

Report

Report Number
2936485-2011-00256
Event Type
Malfunction
Date Received
April 26, 2011
Date of Event
April 1, 2011
Report Date
April 1, 2011
Manufacturer
STRYKER ENDOSCOPY SAN JOSE
Product Code
FCW
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GA, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

ADD'L INFO WILL BE PROVIDED ONCE THE INVESTIGATION IS COMPLETED.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE POWER ON THE UNIT SHUTS OFF AFTER A FEW MINUTES.

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