FDA Adverse Event Malfunction Summary report: N

X7000 XENON LIGHTSOURCE

MDR report key: 2190631 · Received July 27, 2011

Report

Report Number
2936485-2011-00541
Event Type
Malfunction
Date Received
July 27, 2011
Date of Event
July 13, 2011
Report Date
July 13, 2011
Manufacturer
STRYKER ENDOSCOPY SAN JOSE
Product Code
FCW
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AZ, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

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

Description of Event or Problem · 1

IT WAS REPORTED THAT THE UNIT INTERMITTENTLY SHUTS DOWN.

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