FDA Adverse Event Malfunction Summary report: N

PATIENT ESSENTIALS KIT

MDR report key: 1172207 · Received September 11, 2008

Report

Report Number
1644487-2008-02235
Event Type
Malfunction
Date Received
September 11, 2008
Date of Event
August 14, 2008
Report Date
August 14, 2008
Manufacturer
CYBERONICS, INC.
Product Code
LYJ
PMA / PMN Number
P970003
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, 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 A VNS PATIENT'S WRIST MAGNET WAS CRACKED. IT IS UNKNOWN HOW TO THE MAGNET BECAME CRACKED. GOOD FAITH ATTEMPTS TO OBTAIN ADDITIONAL INFORMATION HAVE BEEN UNSUCCESSFUL TO DATE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PATIENT ESSENTIALS KIT LYJ CYBERONICS, INC. 388034

Patients

Seq Age Sex Outcome Treatment
1 36 YR