FDA Adverse Event Malfunction Summary report: N

PROGRAMMING WAND

MDR report key: 1810732 · Received February 29, 2008

Report

Report Number
1644487-2008-00591
Event Type
Malfunction
Date Received
February 29, 2008
Date of Event
January 31, 2008
Report Date
February 1, 2008
Manufacturer
CYBERONICS, INC.
Product Code
LYJ
PMA / PMN Number
P970003
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MS, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

DEVICE FAILURE IS SUSPECTED, BUT DID NOT CAUSE OR CONTRIBUTE TO A DEATH OR SERIOUS INJURY.

Description of Event or Problem · 1

REPORTER INDICATED THAT THE (B)(6) HANDHELD EXPERIENCED BATTERY FAILURE IN THE OPERATING ROOM. (B)(6) HANDHELD WAS REPLACED. ATTEMPTS FOR FURTHER INFORMATION ARE IN PROGRESS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PROGRAMMING WAND LYJ CYBERONICS, INC. 250

Patients

Seq Age Sex Outcome Treatment
1