FDA Adverse Event Malfunction Summary report: N

HEARTSINE SAMARITAN 300P AND PAD PAK

MDR report key: 3880077 · Received May 6, 2014

Report

Report Number
3004123209-2014-00434
Event Type
Malfunction
Date Received
May 6, 2014
Date of Event
April 23, 2014
Report Date
April 28, 2014
Manufacturer
HEARTSINE TECHNOLOGIES, LTD
Product Code
MKJ
PMA / PMN Number
K123881
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SW
Reporter Occupation
NOT APPLICABLE

Narratives

Description of Event or Problem · 1

THERE WAS NO PATIENT INVOLVED IN THIS EVENT. THIS DEVICE MALFUNCTIONED BECAUSE THE RED STATUS INDICATOR WAS FLASHING AND BEEPING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
270691 HEARTSINE SAMARITAN 300P AND PAD PAK AUTOMATED EXTERNAL DEFIBRILLATOR MKJ HEARTSINE TECHNOLOGIES, LTD PAD

Patients

Seq Age Sex Outcome Treatment
1