FDA Adverse Event Malfunction Summary report: N

HEART START XL

MDR report key: 1983685 · Received February 3, 2011

Report

Report Number
1218950-2011-00296
Event Type
Malfunction
Date Received
February 3, 2011
Report Date
January 7, 2011
Manufacturer
PHILIPS HEALTHCARE
Product Code
MKJ
PMA / PMN Number
K001725
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4).

Description of Event or Problem · 1

THE CUSTOMER REPORTED THAT THE DEVICE DID NOT DISCHARGE ENERGY AS EXPECTED DURING CARDIOVERSION. THERE WAS NO REPORT OF NEGATIVE PATIENT OUTCOME.

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