FDA Adverse Event Malfunction Summary report: N

SWITCHED INTERNAL PADDLES -4.5CM

MDR report key: 3810180 · Received February 4, 2014

Report

Report Number
1218950-2014-00497
Event Type
Malfunction
Date Received
February 4, 2014
Report Date
January 9, 2014
Manufacturer
PHILIPS MEDICAL SYSTEMS
Product Code
LDD
PMA / PMN Number
K954957
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). A FOLLOW UP REPORT WILL BE SUBMITTED UPON COMPLETION OF THE INVESTIGATION.

Description of Event or Problem · 1

THE CUSTOMER REPORTED THAT THE INTERNAL PADDLES DON'T WORK AND THE HANDLES ARE COMING APART. THERE WAS NO PT INVOLVEMENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
73636 SWITCHED INTERNAL PADDLES -4.5CM LDD, MKJ, DQA LDD PHILIPS MEDICAL SYSTEMS M4743A 5-2013

Patients

Seq Age Sex Outcome Treatment
1