FDA Adverse Event Injury Summary report: N

INSYNC III

MDR report key: 6006021 · Received October 6, 2016

Report

Report Number
9614453-2016-05988
Event Type
Injury
Date Received
October 6, 2016
Date of Event
July 28, 2016
Report Date
July 28, 2016
Manufacturer
IPG MFG SWITZERLAND
Product Code
LWP
PMA / PMN Number
P010015
Removal / Correction Number
Z-0342-2016
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

PRODUCT EVENT SUMMARY: PRELIMINARY AND FUNCTIONAL TESTING WAS PERFORMED ON THE RETURNED DEVICE. RESULTS CONFIRMED NORMAL PACING AND SENSING FUNCTIONALITY. INTERNAL BATTERY IMPEDANCE DURING FUNCTIONAL TESTING WAS FOUND TO BE HIGHER THAN THE THRESHOLD ESTABLISHED FOR AUTOMATED TESTING. HOWEVER, THE MEASURED IMPEDANCE IN THE BATTERY HAD NOT REACHED A LEVEL TO IMPACT DEVICE PERFORMANCE. THIS DEVICE WAS REPORTED AS INCLUDED IN THE FIELD ACTION NOTED BUT RETURNED PRODUCT INVESTIGATION FOUND THE DEVICE DID NOT PERFORM AS DESCRIBED IN THE FIELD ACTION. THE DEVICE IS NO LONGER INCLUDED AS PART OF THE FIELD ACTION. CONCOMITANT MEDICAL PRODUCTS: 419488 LEAD, IMPLANTED: (B)(6) 2008. A GOOD FAITH EFFORT WILL BE MADE TO OBTAIN THE APPLICABLE INFORMATION RELEVANT TO THE REPORT. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE CARDIAC RESYNCHRONIZATION THERAPY PACEMAKER (CRT-P) WAS PROPHYLACTICALLY REPLACED. REPLACEMENT WAS INITIATED TO PRECLUDE PERMANENT IMPAIRMENT OF A BODY FUNCTION OR PERMANENT DAMAGE TO A BODY STRUCTURE. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
659340 INSYNC III PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE LWP IPG MFG SWITZERLAND 8042B

Patients

Seq Age Sex Outcome Treatment
1 90 YR Hospitalization| R 1488T LEAD, 1488T LEAD