SYNCARDIA FREEDOM DRIVER 595000-001

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a other report with the FDA on 2020-02-14 for SYNCARDIA FREEDOM DRIVER 595000-001 manufactured by Syncardia Systems, Llc.

Event Text Entries

[188659298] The results of the investigation will be provided in a follow-up mdr. Ce (b)(4) initial.
Patient Sequence No: 1, Text Type: N, H10


[188659299] During a routine evaluation, a syncardia technician reported that the freedom driver ran on the secondary motor and exhibited a fault alarm.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3003761017-2020-00051
MDR Report Key9711392
Report SourceOTHER
Date Received2020-02-14
Date of Report2020-02-13
Date of Event2020-01-15
Date Mfgr Received2020-01-15
Device Manufacturer Date2018-01-04
Date Added to Maude2020-02-14
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. KERRI HENSLEY
Manufacturer Street1992 E. SILVERLAKE ROAD
Manufacturer CityTUCSON, AZ
Manufacturer CountryUS
Manufacturer Phone5451234120
Manufacturer G1SYNCARDIA SYSTEMS, LLC
Manufacturer Street1992 E. SILVERLAKE ROAD
Manufacturer CityTUCSON, AZ
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSYNCARDIA FREEDOM DRIVER
Generic NameEXTERNAL PNEUMATIC DRIVER
Product CodeLOZ
Date Received2020-02-14
Model Number595000-001
Catalog Number595000-001
Device AvailabilityY
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSYNCARDIA SYSTEMS, LLC
Manufacturer Address1992 E. SILVERLAKE ROAD TUCSON, AZ US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-14

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