SOLARA QUAD CRT-P MRI SURESCAN W4TR03

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 2020-03-28 for SOLARA QUAD CRT-P MRI SURESCAN W4TR03 manufactured by Medtronic Puerto Rico Operations Co..

Event Text Entries

[185359780] Concomitant medical products: fr995-29, aortic valve, implanted: (b)(6) 2019. If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


[185359781] It was reported that the cardiac resynchronization therapy pacemaker (crt-p) system was explanted and replaced due to infection. No further patient complications have been reported as a result of this event.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3004209178-2020-06315
MDR Report Key9893176
Report SourceOTHER
Date Received2020-03-28
Date of Report2020-03-28
Date of Event2019-12-17
Date Mfgr Received2020-03-11
Device Manufacturer Date2018-02-14
Date Added to Maude2020-03-28
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 ST NE
Manufacturer CityMOUNDS VIEW MN 55112
Manufacturer CountryUS
Manufacturer Postal55112
Manufacturer Phone7635055378
Manufacturer G1MEDTRONIC PUERTO RICO OPERATIONS CO.
Manufacturer StreetROAD 31, KM. 24, HM 4 CEIBA NORTE INDUSTRIAL PARK
Manufacturer CityJUNCOS PR 00777
Manufacturer CountryUS
Manufacturer Postal Code00777
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSOLARA QUAD CRT-P MRI SURESCAN
Generic NamePULSE GENERATOR, PACEMAKER, IMPLANTABLE, WITH CARDIAC RESYNCHRONIZATION
Product CodeNKE
Date Received2020-03-28
Model NumberW4TR03
Catalog NumberW4TR03
Device Expiration Date2019-08-14
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerMEDTRONIC PUERTO RICO OPERATIONS CO.
Manufacturer AddressROAD 31, KM. 24, HM 4 CEIBA NORTE INDUSTRIAL PARK JUNCOS PR 00777 US 00777


Patients

Patient NumberTreatmentOutcomeDate
150761. Hospitalization; 2. Required No Informationntervention 2020-03-28

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