FDA Adverse Event Death Summary report: N

SYNCARDIA FREEDOM DRIVER

MDR report key: 4538072 · Received February 18, 2015

Report

Report Number
3003761017-2015-00069
Event Type
Death
Date Received
February 18, 2015
Date of Event
January 16, 2015
Report Date
January 16, 2015
Manufacturer
SYNCARDIA SYSTEMS, INC.
Product Code
LOZ
PMA / PMN Number
P030011
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

THE FREEDOM DRIVERS HAVE BEEN RETURNED TO SYNCARDIA FOR EVAL. AN INVESTIGATION HAS BEEN INITIATED AND PRELIMINARY RESULTS INDICATED THAT THE DRIVERS PERFORMED AS INTENDED AND THERE IS NO EVIDENCE OF A DEVICE MALFUNCTION. WHEN THE INVESTIGATION HAS BEEN COMPLETED, THE RESULTS WILL BE PROVIDED IN A SUPPLEMENTAL MDR.

Description of Event or Problem · 1

THE REPORTED ISSUE INVOLVES THREE FREEDOM DRIVERS AND ARE REPORTED UNDER THREE SEPARATE MEDICAL DEVICE REPORTS: FREEDOM DRIVER SN (B)(4) (MFR REPORT # 3003761017-2015-00067); FREEDOM DRIVER SN (B)(4) (MFR REPORT # 3003761017-2015-00068); AND FREEDOM DRIVER SN (B)(4). THE CUSTOMER REPORTED THAT ALL THREE FREEDOM DRIVERS EXHIBITED FAULT ALARMS WHILE SUPPORTING A PT AT HOME. THE CUSTOMER ALSO REPORTED THAT THE PT, WHO WAS AT HOME, WAS UNCONSCIOUS WITH LABORED BREATHING WHEN THE FIRST DRIVER EXHIBITED A FAULT ALARM. THE PT WAS TRANSPORTED TO THE EMERGENCY ROOM AT (B)(6) AND SWITCHED TO THE SECOND FREEDOM DRIVER. THE SECOND FREEDOM DRIVER EXHIBITED A FAULT ALARM AND THE PT WAS SWITCHED TO THE THIRD FREEDOM DRIVER. THIRD FREEDOM DRIVER EXHIBITED A FAULT ALARM. THE PT SUBSEQUENTLY EXPIRED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
118026 SYNCARDIA FREEDOM DRIVER CIRCULATORY ASSIST DEVICE LOZ SYNCARDIA SYSTEMS, INC.

Patients

Seq Age Sex Outcome Treatment
1 36 YR