FDA Adverse Event Death Summary report: N

FR2

MDR report key: 1723323 · Received June 10, 2010

Report

Report Number
3030677-2010-00075
Event Type
Death
Date Received
June 10, 2010
Date of Event
May 8, 2010
Report Date
June 10, 2010
Manufacturer
PHILIPS MEDICAL SYSTEMS, HEARTSTREAM
Product Code
MKJ
PMA / PMN Number
003565
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

EVAL PENDING.

Description of Event or Problem · 1

PT DEATH DURING AED DEPLOYMENT. USER INDICATES ISSUE WITH PADS CONTACT. (B) (4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 FR2 AED MKJ PHILIPS MEDICAL SYSTEMS, HEARTSTREAM M3860A-ABA

Patients

Seq Age Sex Outcome Treatment
1 65 YR Death