FDA Adverse Event Injury Summary report: N

DEXTRUS 4136

MDR report key: 3010543 · Received March 19, 2013

Report

Report Number
1028232-2013-00696
Event Type
Injury
Date Received
March 19, 2013
Date of Event
January 4, 2013
Report Date
March 5, 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 DEVICE WAS NOT RETURNED FOR ANALYSIS. THE ANALYSIS IS THEREFORE BASED ON THE INSPECTION OF THE QUALITY DOCUMENTS ASSOCIATED WITH THE MANUFACTURE OF THIS PARTICULAR DEVICE. THE MANUFACTURING PROCESS FOR THIS DEVICE 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. IN SUMMARY, THE DEVICE WAS NOT RETURNED FOR ANALYSIS. THE REVIEW OF THE QUALITY DOCUMENTS CONFIRMED A REGULAR DEVICE MANUFACTURING.

Description of Event or Problem · 1

BOSTON SCIENTIFIC RECEIVED INFORMATION THAT THIS RIGHT VENTRICULAR LEAD DISPLAYED INCREASED PACING THRESHOLD MEASUREMENTS AND A LOSS OF CAPTURE AT MAXIMUM OUTPUTS. THE PHYSICIAN DECIDED TO REPOSITION THE LEAD. THERE WERE NO ADVERSE PATIENT EFFECTS REPORTED. PATIENT HAD UNDERLYING RHYTHM. THE LEAD REMAINS IMPLANTED SUCCESSFULLY REPOSITIONED. AS NO FURTHER INFORMATION CONCERNING THIS REPORT IS EXPECTED, OUR INVESTIGATION IS COMPLETE. THIS INVESTIGATION WILL BE UPDATED SHOULD FURTHER INFORMATION BE PROVIDED. AN EXPLANT DATE WAS PROVIDED FOR THIS DEVICE, BUT THE EVENT STATES THE LEAD WAS REPOSITIONED AND REMAINS IMPLANTED. NO DEVICE WAS RETURNED FOR ANALYSIS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
114151 DEXTRUS 4136 PACER LEAD NVN BIOTRONIK SE & CO. KG 358754

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization