FDA Adverse Event Malfunction Summary report: N

HEART START XL

MDR report key: 1874443 · Received October 12, 2010

Report

Report Number
1218950-2010-01931
Event Type
Malfunction
Date Received
October 12, 2010
Report Date
September 15, 2010
Manufacturer
PHILIPS HEALTHCARE
Product Code
MKJ
PMA / PMN Number
K001725
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SP
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). ON (B)(6) 2010 THE CUSTOMER REPORTED THE PADDLE SET WAS INTERMITTENTLY DISCHARGING DURING TESTING. THIS COMPLAINT IS STILL BEING INVESTIGATED. A FOLLOW-UP REPORT WILL BE SUBMITTED UPON COMPLETION OF THE INVESTIGATION.

Description of Event or Problem · 1

ON (B)(6) 2010 THE CUSTOMER REPORTED THE PADDLE SET WAS INTERMITTENTLY DISCHARGING DURING TESTING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 HEART START XL MKJ PHILIPS HEALTHCARE M4735A

Patients

Seq Age Sex Outcome Treatment
1