CENTRIMAG MOTOR, OUS 201-10002

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign report with the FDA on 2018-08-11 for CENTRIMAG MOTOR, OUS 201-10002 manufactured by Thoratec Switzerland Gmbh.

Event Text Entries

[116865748] No patient information. The device returned for analysis. The complaint investigation determined the reported difficulty was the result of a design related wear issue. After review of this event and similar incidents, abbott has decided to initiate a voluntary field action for centrimag. Abbott performed a comprehensive investigation which included device analysis, manufacturing evaluation and trend analysis.
Patient Sequence No: 1, Text Type: N, H10


[116865749] It was reported that the primary console displayed a "system fault" error message. The error message appeared after having been connected to motor and flow probe during a demonstration. No patient was involved. This event was previously not reported due to no patient involvement. Abbott made the decision on july 13, 2018 to initiate a voluntary recall, therefore this event is being upgraded to reportable.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2916596-2018-03423
MDR Report Key7775410
Report SourceFOREIGN
Date Received2018-08-11
Date of Report2018-08-11
Date of Event2008-03-19
Date Mfgr Received2018-07-13
Date Added to Maude2018-08-11
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 ContactMR. BOB FRYC
Manufacturer Street6035 STONERIDGE DRIVE
Manufacturer CityPLEASANTON CA 94588
Manufacturer CountryUS
Manufacturer Postal94588
Manufacturer Phone7818528204
Manufacturer G1THORATEC SWITZERLAND GMBH
Manufacturer StreetTECHNOPARKSTRASSE 1
Manufacturer CityZURICH CH-8005
Manufacturer CountrySZ
Manufacturer Postal CodeCH-8005
Single Use3
Remedial ActionRC
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCENTRIMAG MOTOR, OUS
Generic NameMOTOR
Product CodeDSW
Date Received2018-08-11
Returned To Mfg2008-06-16
Catalog Number201-10002
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerTHORATEC SWITZERLAND GMBH
Manufacturer AddressTECHNOPARKSTRASSE 1 ZURICH CH-8005 SZ CH-8005


Patients

Patient NumberTreatmentOutcomeDate
10 2018-08-11

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.