FDA Adverse Event Injury Summary report: N

SELOX ST 60

MDR report key: 3211823 · Received July 8, 2013

Report

Report Number
1028232-2013-01864
Event Type
Injury
Date Received
July 8, 2013
Date of Event
May 13, 2013
Report Date
June 27, 2013
Manufacturer
BIOTRONIK SE & CO. KG
Product Code
NVN
PMA / PMN Number
P950037
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
GM
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE LEAD UNDER COMPLAINT WAS NOT RETURNED FOR ANALYSIS. THE ANALYSIS IS THEREFORE BASED ON THE INSPECTION OF THE QUALITY DOCUMENTS ASSOCIATED WITH THE MANUFACTURE OF THIS PARTICULAR LEAD AS WELL AS THE HOME MONITORING DATA RETURNED FOR ANALYSIS. THE MANUFACTURING PROCESS FOR THIS LEAD WAS RE-INVESTIGATED. ALL PRODUCTION STEPS HAD BEEN PERFORMED ACCORDINGLY. THERE WAS NO SIGN OF ANY INCONSISTENCY DURING THE MANUFACTURING PROCESS WHICH MIGHT BE RELATED TO THE CLINICAL OBSERVATION. THE RETURNED DATA WERE ANALYZED. THE INSPECTION REVEALED A SLOWLY INCREASING VENTRICULAR PACING IMPEDANCE WITH VALUES UP TO > 2000 OHM, AS INDICATED IN THE COMPLAINT DESCRIPTION. IN SUMMARY, THE LEAD WAS NOT RETURNED FOR ANALYSIS. BASED ON THE INFORMATION AVAILABLE FOR ANALYSIS, NO CONCLUSIONS CAN BE DRAWN REGARDING THE ROOT CAUSE OF THE CLINICAL OBSERVATION. THE REVIEW OF THE QUALITY DOCUMENTS CONFIRMED A REGULAR LEAD MANUFACTURING.

Description of Event or Problem · 1

OUS MDR - SLOWLY INCREASING VENTRICULAR IMPEDANCE (>2000 OHMS) LEADING TO EXIT BLOCK WERE REPORTED BY HOME MONITORING AND CONFIRMED DURING A FOLLOW-UP. THE EXPLANTATION OF THE LEAD IS PLANNED. THIS IS ALL OF THE AVAILABLE INFORMATION AT THIS TIME. IF ADDITIONAL INFORMATION BECOMES AVAILABLE, THIS EVENT WILL BE UPDATED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
309077 SELOX ST 60 PACER LEAD NVN BIOTRONIK SE & CO. KG 346367

Patients

Seq Age Sex Outcome Treatment
1 Other