FDA Adverse Event Malfunction Summary report: N

HEART START XL

MDR report key: 1930504 · Received November 30, 2010

Report

Report Number
1218950-2010-02416
Event Type
Malfunction
Date Received
November 30, 2010
Report Date
November 1, 2010
Manufacturer
PHILIPS HEALTHCARE
Product Code
MKJ
PMA / PMN Number
K001725
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

(B)(4): THE CUSTOMER REPORTED THAT THE UNIT FAILED TO POWER UP. ON (B)(6) 2010, THE CUSTOMER REPORTED TO PHILIPS THAT REPLACING THE CONTROL PCA RESOLVED THE POWER FAILURE. AS OF 11/22/2010, THERE HAVE BEEN NO FURTHER REPORTS FROM THIS CUSTOMER CONCERNING THIS FAILURE WITH THIS DEVICE. THE UNIT REMAINS AT THE CUSTOMER SITE.

Description of Event or Problem · 1

THE CUSTOMER REPORTED THAT THE UNIT FAILED TO POWER UP.

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