FDA Adverse Event Malfunction Summary report: N

HEARTSINE SAMARITAN 300P AND PAD PAK

MDR report key: 5437752 · Received February 16, 2016

Report

Report Number
3004123209-2016-00237
Event Type
Malfunction
Date Received
February 16, 2016
Date of Event
February 10, 2016
Report Date
April 14, 2016
Manufacturer
HEARTSINE TECHNOLOGIES LTD
Product Code
MKJ
PMA / PMN Number
K041067
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
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 HISTORY LOG SHOWED THE PAD-PAK WAS FIRST INSTALLED SUCCESSFULLY ON THE (B)(6) 2011 AND PERFORMED TO SPECIFICATION UP TO THE (B)(6) 2015. BETWEEN THE (B)(6) 2015 THE DEVICE RECORDS 3 MANUAL POWER UPS ALL OF TEN MINUTES DURATION. THE DEVICE PERFORMS SUCCESSFUL SELF-TESTS UP TO THE (B)(6) 2016. THE RETURNED PAD-PAK WAS INSERTED INTO THE DEVICE AND PASSED A SELF-TEST. NO WARNINGS WERE GIVEN AT SHUTDOWN AND THE STATUS LED CONTINUED TO FLASH GREEN. A TEST SHOCK WAS DELIVERED WITHOUT FAULT DURING TESTING. INVESTIGATION WAS UNABLE TO REPLICATE THE REPORTED FAULT. THE MANUAL POWER UPS MAY INDICATE THE USER WAS REGULARLY POWER CYCLING THE DEVICE OR THE BEGINNINGS OF MEMBRANE FAILURE. AT NO TIME DURING TESTING WAS THE DEVICE OBSERVED SWITCHING ON AUTOMATICALLY.

Additional Manufacturer Narrative · 0

EXEMPTION NUMBER E2015058 HEARTSINE TECHNOLOGIES LTD (MANUFACTURER) IS SUBMITTING THE REPORT ON BEHALF OF HEARTSINE TECHNOLOGIES LLC (IMPORTER). H3 OTHER TEXT : NOT YET RETURNED TO MANUFACTURER

Description of Event or Problem · 0

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

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
95334 HEARTSINE SAMARITAN 300P AND PAD PAK AUTOMATED EXTERNAL DEFIBRILLATOR MKJ HEARTSINE TECHNOLOGIES LTD SAM N/A

Patients

Seq Age Sex Outcome Treatment
1