FDA Adverse Event Malfunction Summary report: N

RELIA DR

MDR report key: 2131605 · Received June 16, 2011

Report

Report Number
6000094-2011-01173
Event Type
Malfunction
Date Received
June 16, 2011
Date of Event
April 15, 2011
Manufacturer
MEDTRONIC S.A.
Product Code
NVZ
PMA / PMN Number
P980035/S097
Removal / Correction Number
ASKU
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PL
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), THE DEVICE WAS RETURNED AND ANALYZED. NO ANOMALIES WERE FOUND. IT WAS NOTED THE PACKAGING WAS DAMAGED.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE DEVICE ARRIVED AT THE HOSPITAL WITH BROKEN PLASTIC CASE AND STERILE PACKAGE INTEGRITY WAS SUSPECTED TO BE DAMAGED. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE DEVICE ARRIVED AT THE HOSPITAL WITH BROKEN PLASTIC CASE AND STERILE PACKAGE INTEGRITY WAS SUSPECTED TO BE DAMAGED. THE DEVICE WAS NEVER CONSIDERED FOR IMPLANTATION. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 RELIA DR IMPLANTABLE PULSE GENERATOR NVZ MEDTRONIC S.A. REDR01 ASKU

Patients

Seq Age Sex Outcome Treatment
1 Other