SYNCARDIA FREEDOM POWER ADAPTOR 295070-001

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign report with the FDA on 2020-02-18 for SYNCARDIA FREEDOM POWER ADAPTOR 295070-001 manufactured by Syncardia Systems, Llc.

MAUDE Entry Details

Report Number3003761017-2020-00066
MDR Report Key9722244
Report SourceDISTRIBUTOR,FOREIGN
Date Received2020-02-18
Date of Report2020-02-06
Date of Event2020-01-30
Date Mfgr Received2020-01-30
Date Added to Maude2020-02-18
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 85713
Manufacturer CountryUS
Manufacturer Postal85713
Manufacturer Phone5205451234
Manufacturer G1SYNCARDIA SYSTEMS, LLC
Manufacturer Street1992 E. SILVERLAKE ROAD
Manufacturer CityTUCSON AZ 85713
Manufacturer CountryUS
Manufacturer Postal Code85713
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSYNCARDIA FREEDOM POWER ADAPTOR
Generic NameAC POWER ADAPTOR
Product CodeLOZ
Date Received2020-02-18
Catalog Number295070-001
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSYNCARDIA SYSTEMS, LLC
Manufacturer Address1992 E. SILVERLAKE ROAD TUCSON AZ 85713 US 85713


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-18

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