FDA Adverse Event Injury Summary report: N

EON MINI

MDR report key: 3862836 · Received May 23, 2014

Report

Report Number
1627487-2014-01330
Event Type
Injury
Date Received
May 23, 2014
Date of Event
April 28, 2014
Report Date
April 28, 2014
Manufacturer
ST. JUDE MEDICAL - NEUROMODULATION
Product Code
GZB
PMA / PMN Number
P010032
Removal / Correction Number
1627487-07262012-002-R,
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

RECALL NUMBERS: 1627487-05242011-002-R, 1627487-07262012-001-C. THIS IPG SERIAL NUMBER WAS INCLUDED IN FIELD ADVISORIES AND A FIELD CORRECTION. SJM 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. SJM DEFERS TO THE PATIENT'S PHYSICIAN REGARDING MEDICAL HISTORY.

Description of Event or Problem · 1

DEVICE 1 OF 2 REFERENCE MFR REPORT #1627487-2014-01331. IT WAS REPORTED THE PT EXPERIENCED POCKET HEATING WHILE RECHARGING. THE PT HAS NOT CHARGED THE IPG IN SEVERAL MONTHS DUE TO THE HEATING ISSUE AND A PREVIOUS SPINAL FUSION PROCEDURE. FOLLOW UP ON THIS MATTER FOUND THE PT IS CURRENTLY WITHOUT STIMULATION AND UNABLE TO COMMUNICATE WITH HIS IPG USING EITHER THE CHARGING SYSTEM OR PROGRAMMER. AN SJM REP HAS BEEN CONTACTED TO FURTHER INTERROGATE THE PT'S IPG. ON 08/01/2012 ST. JUDE MEDICAL, NEUROMODULATION DIVISION, SENT FIELD ACTION LETTERS TO PTTS RELATED TO HEATING WHILE CHARGING AND RAISED AWARENESS OF THIS ISSUE TO PTS. AN INCREASE IN PRIOR NON-REPORTED HEATING WHILE CHARGING EVENTS AND OTHER NON-REPORTED EVENTS WAS EXPECTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
309252 EON MINI SC SIPG GZB ST. JUDE MEDICAL - NEUROMODULATION 3788 3161513

Patients

Seq Age Sex Outcome Treatment
1 42 YR Other IMPLANT DATE:| SCS LEAD, MODEL 3186 (2),