FDA Adverse Event Malfunction Summary report: N

PROGRAMMING SOFTWARE

MDR report key: 1133180 · Received August 22, 2008

Report

Report Number
1644487-2008-01989
Event Type
Malfunction
Date Received
August 22, 2008
Date of Event
January 1, 2008
Report Date
July 25, 2008
Manufacturer
CYBERONICS, INC.
Product Code
LYJ
PMA / PMN Number
P970003
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
ID, 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

IT WAS REPORTED THAT THE SERIAL CABLE CORD THAT PLUGS INTO THE HANDHELD HAS A LOOSE CONNECTION. A REPLACEMENT WAS SENT TO THE SITE. PRODUCT ANALYSIS IS PENDING ON THE HANDHELD.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PROGRAMMING SOFTWARE LYJ CYBERONICS, INC. 250 584947

Patients

Seq Age Sex Outcome Treatment
1