FDA Adverse Event Malfunction Summary report: N

CAPSUREFIX NOVUS MRI

MDR report key: 2131570 · Received June 16, 2011

Report

Report Number
2649622-2011-10517
Event Type
Malfunction
Date Received
June 16, 2011
Date of Event
April 28, 2011
Manufacturer
MEDTRONIC PUERTO RICO, INC.
Product Code
NVN
PMA / PMN Number
P090013
Removal / Correction Number
ASKU
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IT
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

THIS EVENT OCCURRED OUTSIDE THE US. ALL INFORMATION PROVIDED IS INCLUDED IN THIS REPORT. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. PATIENT INFORMATION IS NOT GENERALLY AVAILABLE DUE TO CONFIDENTIALITY CONCERNS. ANALYSIS OF THE DEVICE IS IN PROCESS; THE RESULTS WILL BE FORWARDED WHEN AVAILABLE.

Additional Manufacturer Narrative · 1

THIS EVENT OCCURRED OUTSIDE THE US. ALL INFORMATION PROVIDED IS INCLUDED IN THIS REPORT. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. PATIENT INFORMATION IS NOT GENERALLY AVAILABLE DUE TO CONFIDENTIALITY CONCERNS. EVALUATION SUMMARY: (B)(4): NO ANOMALIES FOUND; FULL LEAD RETURNED AND ANALYZED.

Description of Event or Problem · 1

IT WAS REPORTED THAT DURING IMPLANT OF THE LEAD IT WAS NOT POSSIBLE TO EXTEND THE DISTAL HELIX OUT OF THE LEAD TIP. THEREFORE THE LEAD WAS NOT IMPLANTED AND REPLACED WITH A NEW LEAD. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

Description of Event or Problem · 1

IT WAS REPORTED THAT DURING IMPLANT OF THE LEAD IT WAS NOT POSSIBLE TO EXTEND THE DISTAL HELIX OUT OF THE LEAD TIP. THEREFORE THE LEAD WAS NOT IMPLANTED AND REPLACED WITH A NEW LEAD. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CAPSUREFIX NOVUS MRI IMPLANTABLE PACING LEAD NVN MEDTRONIC PUERTO RICO, INC. 5086MRI ASKU

Patients

Seq Age Sex Outcome Treatment
1 Other