FDA Adverse Event Injury Summary report: N

EON IPG

MDR report key: 1790646 · Received August 6, 2010

Report

Report Number
1627487-2010-01522
Event Type
Injury
Date Received
August 6, 2010
Date of Event
November 5, 2009
Report Date
November 6, 2009
Manufacturer
ADVANCED NEUROMODULATION SYSTEMS, INC.
Product Code
LGW
PMA / PMN Number
P010032
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

EVALUATION: THE DEVICE HISTORY AND STERILIZATION RECORDS WERE REVIEWED. RESULTS: THE DEVICE HISTORY AND STERILIZATION RECORDS REVIEWED WERE FOUND TO MEET SPECS AND NO ANOMALIES WERE FOUND. CONCLUSION: THE CAUSE OF THE REPORTED COMPLAINT COULD NOT BE DETERMINED FROM THE REVIEW OF THE DHR AND STERILIZATION RECORDS. THIS MDR IS BEING SUBMITTED PAST THE 30 DAY REPORTING REQUIREMENT AS PART OF A RETROSPECTIVE REVIEW INITIATED IN RESPONSE TO AN FDA INSPECTION. A RETROSPECTIVE REVIEW OF THE COMPLAINT RECORD DETERMINED THAT ANS MISINTERPRETED THE MDR REGULATIONS IN THIS INSTANCE. ANS HAS LIMITED INFORMATION RELATED TO THE PATIENT'S MEDICAL HISTORY AND IS UNABLE TO FORM AN OPINION AS TO THE RELEVANCY OF THE PATIENT'S HISTORY TO THE EVENT REPORTED. ANS DEFERS TO THE PATIENT'S PHYSICIAN REGARDING MEDICAL HISTORY.

Description of Event or Problem · 1

THE PT RECEIVED HER SCS SYSTEM ON (B)(6)2008. IT WAS REPORTED THAT THE PT EXPERIENCED HEATING AT IMPLANT SITE. IT WAS REPORTED THAT THE PT REQUESTED TO HAVE HER IPG REPLACED, BUT NO EXPLANTED DEVICES FROM THIS PT HAVE BEEN RETURNED TO THE MFR FOR ANALYSIS. NO FURTHER INFO IS AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 EON IPG TOTALLY IMPLANTABLE PULSE GENERATOR LGW ADVANCED NEUROMODULATION SYSTEMS, INC. 3716 116853

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention