FDA Adverse Event Malfunction Summary report: N

HEARTSINE SAMARITAN 350P AND PAD PAK

MDR report key: 6816107 · Received August 24, 2017

Report

Report Number
3004123209-2017-00858
Event Type
Malfunction
Date Received
August 24, 2017
Date of Event
August 1, 2017
Report Date
September 28, 2017
Manufacturer
HEARTSINE TECHNOLOGIES LTD
Product Code
MKJ
PMA / PMN Number
P160008
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GM
Reporter Occupation
PATIENT

Narratives

Additional Manufacturer Narrative · 0

EXEMPTION NUMBER E2015058. HEARTSINE TECHNOLOGIES LTD (MANUFACTURER) IS SUBMITTING THE REPORT ON BEHALF OF HEARTSINE TECHNOLOGIES LLC (IMPORTER). THE DEVICE HISTORY RECORDS FOR THE RETURNED SAM 350P DEVICE WERE REVIEWED AND THIS CONFIRMED THAT ALL MANUFACTURING AND QUALITY CHECKS AND TESTS HAD BEEN SUCCESSFULLY COMPLETED PRIOR TO THE DISPATCH OF THE SAM 350P FROM HEARTSINE TECHNOLOGIES, BELFAST ON 25TH JANUARY 2016. ON RECEIPT OF THE DEVICE THE HISTORY AND MEMORY LOGS WERE DOWNLOADED. THE HISTORY LOG FOR THIS DEVICE SHOWED THAT THE PAD-PAK WAS FIRST INSTALLED ON (B)(6) 2016 AND THAT IT HAD PERFORMED TO SPECIFICATION UP TO (B)(6) 2017 THE DEVICE WAS TESTED ON THE CALIBRATED IMPULSE DEFIBRILLATOR AND DELIVERED A TEST SHOCK WITHOUT FAULT. THE DEVICE WAS SUCCESSFULLY CONNECTED TO SAVER EVO AFTER EACH TEMPERATURE RANGE AND THE HISTORY AND MEMORY LOGS WERE SUCCESSFULLY DOWNLOADED.

Additional Manufacturer Narrative · 0

EXEMPTION NUMBER E2015058. HEARTSINE TECHNOLOGIES LTD (MANUFACTURER) IS SUBMITTING THE REPORT ON BEHALF OF HEARTSINE TECHNOLOGIES LLC (IMPORTER).

Description of Event or Problem · 0

THERE WAS NO PATIENT INVOLVED IN THIS EVENT. RED STATUS INDICATOR.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
597492 HEARTSINE SAMARITAN 350P AND PAD PAK AUTOMATED EXTERNAL DEFIBRILLATOR MKJ HEARTSINE TECHNOLOGIES LTD SAM

Patients

Seq Age Sex Outcome Treatment
1