SYNCARDIA COMPANION 2 DRIVER 397002-001

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2020-03-17 for SYNCARDIA COMPANION 2 DRIVER 397002-001 manufactured by Syncardia Systems, Llc.

Event Text Entries

[183979237] The companion 2 driver will be returned to syncardia for evaluation. The results of the evaluation will be provided in a follow-up mdr. (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[183979238] The customer, a syncardia certified hospital, reported that the companion 2 driver exhibited compressor cycling while supporting a patient. There was no reported adverse patient impact.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3003761017-2020-00090
MDR Report Key9842220
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2020-03-17
Date of Report2020-03-16
Date of Event2020-03-05
Date Mfgr Received2020-03-05
Device Manufacturer Date2017-09-08
Date Added to Maude2020-03-17
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
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
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSYNCARDIA COMPANION 2 DRIVER
Generic NameEXTERNAL PNEUMATIC DRIVER
Product CodeLOZ
Date Received2020-03-17
Model Number397002-001
Catalog Number397002-001
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 US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-17

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