FDA Adverse Event Injury Summary report: N

ENDOTAK RELIANCE

MDR report key: 2161299 · Received July 13, 2011

Report

Report Number
2124215-2011-07317
Event Type
Injury
Date Received
July 13, 2011
Date of Event
April 14, 2011
Report Date
January 22, 2014
Manufacturer
CPI - DEL CARIBE
Product Code
NVY
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

AS NO FURTHER INFORMATION CONCERNING THIS REPORT IS EXPECTED, OUR INVESTIGATION IS COMPLETE. THIS INVESTIGATION WILL BE UPDATED SHOULD FURTHER INFORMATION BE PROVIDED.

Additional Manufacturer Narrative · 1

ACCORDING TO AVAILABLE INFORMATION, THIS LEAD REMAINS IMPLANTED AND IN SERVICE. SHOULD ADDITIONAL INFORMATION BECOME AVAILABLE, THIS EVENT WILL BE UPDATED.

Description of Event or Problem · 1

DESPITE ATTEMPTS TO OBTAIN ADDITIONAL INFORMATION, NONE COULD BE OBTAINED.

Description of Event or Problem · 1

ADDITIONAL INFORMATION WAS RECEIVED. SUBSEQUENT OUT OF RANGE MEASUREMENTS HAVE BEEN OBSERVED.

Description of Event or Problem · 1

BOSTON SCIENTIFIC RECEIVED INFORMATION THAT LATITUDE RED ALERT WAS GENERATED FOR THIS RIGHT VENTRICULAR LEAD DISPLAYING HIGH OUT OF RANGE SHOCK IMPEDANCE MEASUREMENTS. THE INFORMATION WAS PROVIDED TO THE PATIENT'S PHYSICIAN FOR FURTHER FOLLOW UP. NO ADVERSE PATIENT EFFECTS WERE REPORTED.

Description of Event or Problem · 1

ADDITIONAL INFORMATION WAS RECEIVED. REPORTEDLY, THE IMPEDANCE MEASUREMENTS HAVE BEEN KNOWN TO BE OUT OF RANGE AND A DECISION WAS MADE TO FURTHER MONITOR WITH NO INTERVENTION. IT WAS THOUGHT DEFIBRILLATION THRESHOLD (DFT) TESTING MAY HAVE BEEN PERFORMED OR THE LEAD HAS BEEN OTHERWISE VERIFIED AS BEING FUNCTIONAL. CURRENTLY, THE LEAD IMPEDANCE VARIES AND THE HOSPITAL AND PHYSICIAN ARE AWARE OF THIS ISSUE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ENDOTAK RELIANCE NVY CPI - DEL CARIBE 0293

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention