FDA Adverse Event Injury Summary report: N

EON MINI IMPLANTABLE PULSE GENERATOR

MDR report key: 1971520 · Received January 21, 2011

Report

Report Number
1627487-2011-02078
Event Type
Injury
Date Received
January 21, 2011
Date of Event
December 28, 2010
Report Date
December 28, 2010
Manufacturer
ST. JUDE MEDICAL - NEUROMODULATION
Product Code
LGW
PMA / PMN Number
P010032
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

EVAL, METHOD: THE DEVICE HISTORY AND STERILIZATION RECORDS WERE REVIEWED. RESULTS: THE DEVICE HISTORY AND STERILIZATION RECORDS REVIEWED WERE FOUND TO MEET SPECIFICATIONS 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. 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 MANUFACTURER REPORT: 1627487-2011-02079. THE PATIENT RECEIVED AN SCS SYSTEM, INCLUDING A SURGICAL LEAD AND AN IPG, ON (B)(6) 2010. IT WAS REPORTED THE SCS SYSTEM WAS EXPLANTED LATER THAT MONTH DUE TO INFECTION. AN EXACT EXPLANT DATE WAS NOT PROVIDED BY THE FACILITY. IT IS UNKNOWN IF AND/OR WHEN THE SCS SYSTEM WILL BE REPLACED. THE EXPLANTED PRODUCTS WERE NOT RETURNED TO THE MANUFACTURER FOR ANALYSIS. FOLLOW UP ON THE PATIENT FOUND NO FURTHER ISSUES REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 EON MINI IMPLANTABLE PULSE GENERATOR TOTALLY IMPLANTABLE PULSE GENERATOR LGW ST. JUDE MEDICAL - NEUROMODULATION 3788 3199509

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention