FDA Adverse Event Malfunction Summary report: N

HEART START XL

MDR report key: 2090510 · Received April 19, 2011

Report

Report Number
1218950-2011-01082
Event Type
Malfunction
Date Received
April 19, 2011
Report Date
March 23, 2011
Manufacturer
PHILIPS HEALTHCARE
Product Code
MKJ
PMA / PMN Number
K001725
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FR
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). THE CUSTOMER REPORTED A POWER SUPPLY FAILURE, FAILURE TO POWER UP VIA AC POWER. THE CUSTOMER ORDERED A REPLACEMENT POWER SUPPLY TO RESOLVE THE ISSUE.

Description of Event or Problem · 1

THE CUSTOMER REPORTED A POWER SUPPLY FAILURE, A FAILURE TO POWER UP VIA AC POWER.

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