FDA Adverse Event Injury Summary report: N

EON MINI IPG, 16-CHANNEL RECHARGEABLE

MDR report key: 2329099 · Received November 7, 2011

Report

Report Number
1627487-2011-05391
Event Type
Injury
Date Received
November 7, 2011
Date of Event
October 4, 2011
Report Date
October 4, 2011
Manufacturer
ST. JUDE MEDICAL - NEUROMODULATION
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 RESULTS: THE PRODUCT WAS RECEIVED WITH INSTRUMENT MARKS ON THE CAN. THE IPG COMMUNICATED WITH THE LAB EQUIPMENT. INSPECTION OF THE IPG DID NOT REVEAL ANY ANOMALIES. THE IPG WAS TESTED TO MFG SPECIFICATIONS AND PASSED ALL TESTS. SJM HAS LIMITED INFO RELATED TO THE PT¿S MEDICAL HISTORY AND IS UNABLE TO FORM AN OPINION AS TO THE RELEVANCY OF THE PT¿S HISTORY TO THE EVENT REPORTED. SJM DIFFERS TO THE PT¿S PHYSICIAN REGARDING MEDICAL HISTORY.

Description of Event or Problem · 1

DEVICE 2 OF 2. REFERENCE MFR REPORT#: 1627487-2011-05390. THE PT RECEIVED HER SCS SYSTEM ON (B)(6) 2011, INCLUDING AN IPG AND A PADDLE LEAD. IT WAS REPORTED THE PT WAS NOT RECEIVING ENOUGH PAIN RELIEF. AS A RESULT, THE PT'S IPG AND PADDLE LEAD WERE EXPLANTED. DURING THE SURGICAL PROCEDURE, THE DR NOTICED NUMEROUS EXPOSURES OF THE LEAD, AS WELL AS KINKING OF THE LEAD TAIL. THE DR WAS UNSURE IF THE LEAD'S INSULATION WAS BURNED DUE TO THE EXPLANT PROCEDURE. NO FURTHER INFO IS AVAILABLE AT THIS TIME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 EON MINI IPG, 16-CHANNEL RECHARGEABLE TOTALLY IMPLANTABLE PULSE GENERATOR LGW ST. JUDE MEDICAL - NEUROMODULATION 3788 3218915

Patients

Seq Age Sex Outcome Treatment
1 41 YR Required Intervention SCS LEADS: MODEL 3066 (4)| IMPLANTED:| SCS LEAD EXTENSION: MODEL 3346 (2)| IMPLANTED: