IN.PACT AV ACCESS AVC06004008P

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 2020-03-04 for IN.PACT AV ACCESS AVC06004008P manufactured by Medtronic Ireland.

Event Text Entries

[181980777] If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10


[181980778] During the index procedure, one in. Pact av access was used to treat a lesion located in the anastomosis of the left arm. Approximately 21 months post index procedure, patient suffered from re- stenosis of the left avf. Event was treated with a non-medtronic pta of the anastomosis. Investigator assessed that the event was unlikely to be related to index device, and therapy, but not related to the procedure. Patient recovered.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9612164-2020-00991
MDR Report Key9784911
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-03-04
Date of Report2020-03-04
Date of Event2020-01-15
Date Mfgr Received2020-02-21
Device Manufacturer Date2017-03-08
Date Added to Maude2020-03-04
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 ContactTONI O'DOHERTY
Manufacturer StreetPARKMORE BUSINESS PARK WEST
Manufacturer CityGALWAY
Manufacturer CountryIE
Manufacturer Phone091708734
Manufacturer G1MEDTRONIC IRELAND
Manufacturer StreetPARKMORE BUSINESS PARK WEST
Manufacturer CityGALWAY
Manufacturer CountryIE
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameIN.PACT AV ACCESS
Generic NameDRUG-ELUTING PERIPHERAL TRANSLUMINAL ANGIOPLASTY CATHETER
Product CodeONU
Date Received2020-03-04
Catalog NumberAVC06004008P
Lot NumberV07345648
Device Expiration Date2019-03-08
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerMEDTRONIC IRELAND
Manufacturer AddressPARKMORE BUSINESS PARK WEST GALWAY IE


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-03-04

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