FDA Adverse Event Malfunction Summary report: N

EXTERNAL PADDLES

MDR report key: 2082819 · Received April 29, 2011

Report

Report Number
1218950-2011-01222
Event Type
Malfunction
Date Received
April 29, 2011
Report Date
April 4, 2011
Manufacturer
PHILIPS HEALTHCARE
Product Code
MKJ
PMA / PMN Number
K001725
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GM
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE CUSTOMER REPORTED A DEFECTIVE PADDLE SET. NO PT INVOLVEMENT WAS INDICATED. THIS COMPLAINT IS STILL BEING INVESTIGATED. A FOLLOW-UP REPORT WILL BE SUBMITTED UPON COMPLETION OF THE INVESTIGATION.

Description of Event or Problem · 1

THE CUSTOMER REPORTED A DEFECTIVE PADDLE SET. NO PT INVOLVEMENT WAS INDICATED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 EXTERNAL PADDLES MKJ PHILIPS HEALTHCARE M4746A

Patients

Seq Age Sex Outcome Treatment
1