RING 620RG25 DURAN ANCORE ANNULOPLASTY C

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2020-01-16 for RING 620RG25 DURAN ANCORE ANNULOPLASTY C manufactured by Medtronic Heart Valves Division.

Event Text Entries

[185033111] Product analysis: no product was returned. Conclusion: without the return of the product, no definitive conclusion can be made regarding the clinical observation. If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


[185033112] Medtronic received information that during the implant of this 25mm mitral annuloplasty ring, it was explanted and replaced with a 25mm bioprosthetic mitral valve. The reason for the replacement was not reported. No additional adverse patient effects were reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2025587-2020-00191
MDR Report Key9598453
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-01-16
Date of Report2020-03-12
Date of Event2019-12-18
Date Mfgr Received2020-03-12
Device Manufacturer Date2016-03-28
Date Added to Maude2020-01-16
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 ContactPAULA BIXBY
Manufacturer Street8200 CORAL SEA STREET NE
Manufacturer CityMOUNDS VIEW MN 55112
Manufacturer CountryUS
Manufacturer Postal55112
Manufacturer Phone7635055378
Manufacturer G1MEDTRONIC HEART VALVES DIVISION
Manufacturer Street1851 E DEERE AVE
Manufacturer CitySANTA ANA CA 92705
Manufacturer CountryUS
Manufacturer Postal Code92705
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameRING 620RG25 DURAN ANCORE ANNULOPLASTY C
Generic NameRING, ANNULOPLASTY
Product CodeKRH
Date Received2020-01-16
Model Number620RG25
Catalog Number620RG25
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerMEDTRONIC HEART VALVES DIVISION
Manufacturer Address1851 E DEERE AVE SANTA ANA CA 92705 US 92705


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-01-16

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