FDA Adverse Event Malfunction Summary report: N

HEARTSINE SAMARITAN 350P AND PAD PAK

MDR report key: 6881947 · Received September 21, 2017

Report

Report Number
3004123209-2017-01098
Event Type
Malfunction
Date Received
September 21, 2017
Date of Event
September 11, 2017
Report Date
October 19, 2017
Manufacturer
HEARTSINE TECHNOLOGIES LTD
Product Code
MKJ
PMA / PMN Number
P160008
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NL
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).

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 OF 12TH OCTOBER 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 DISASSEMBLED TO INVESTIGATE. THE MEMBRANE WAS REMOVED AND UPON VISUAL INSPECTION CORROSION WAS OBSERVED ON SEVERAL TRACKS OF THE MEMBRANE TAIL.

Description of Event or Problem · 0

THERE WAS NO PATIENT INVOLVED IN THIS EVENT. DEVICE OBSERVED SWITCHING ON AUTOMATICALLY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
661531 HEARTSINE SAMARITAN 350P AND PAD PAK AUTOMATED EXTERNAL DEFIBRILLATOR MKJ HEARTSINE TECHNOLOGIES LTD SAM

Patients

Seq Age Sex Outcome Treatment
1