ARROW PERCUTANEOUS THROMBOLYTIC DEVICE SET PT-65509

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 2020-02-28 for ARROW PERCUTANEOUS THROMBOLYTIC DEVICE SET PT-65509 manufactured by Arrow International Inc..

Event Text Entries

[181377894] (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[181377895] The customer (user - doctor) reports that the rubber tip of the ptd broke off during normal use within the ifu during a graft declot. The tip was removed in its entirety with myocardial forceps. The doctor reports that there was no excessive force on the rubber tip or device prior to the tip separating. The patient was not harmed.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9680794-2020-00130
MDR Report Key9769729
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-02-28
Date of Report2020-02-10
Date of Event2020-02-05
Date Mfgr Received2020-03-30
Date Added to Maude2020-02-28
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 ContactKATHARINE TARPLEY
Manufacturer Street3015 CARRINGTON MILL BLVD
Manufacturer CityMORRISVILLE NC 27560
Manufacturer CountryUS
Manufacturer Postal27560
Manufacturer Phone9194334854
Manufacturer G1ARROW INTERNATIONAL DE MEXICO S.A. DE C.V.
Manufacturer StreetAVE. WASHINGTON 3701 COLONIA PANAMERICANA, CHIHUAHUA
Manufacturer CityCHIHUAHUA 31200
Manufacturer CountryMX
Manufacturer Postal Code31200
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameARROW PERCUTANEOUS THROMBOLYTIC DEVICE SET
Generic NameCATHETER EMBOLECTOMY
Product CodeDXE
Date Received2020-02-28
Catalog NumberPT-65509
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerARROW INTERNATIONAL INC.
Manufacturer AddressREADING PA


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-28

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