ARROW PERCUTANEOUS THROMBOLYTIC DEVICE KIT PT-65509-HFC

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 2020-03-03 for ARROW PERCUTANEOUS THROMBOLYTIC DEVICE KIT PT-65509-HFC manufactured by Arrow International Inc..

Event Text Entries

[181763919] (b)(4). Additional information received from the doctor at the user facility. Patient with small hematoma. Attempted retrieval but tip in small vein branch and couldn't be retrieved. Tip left in , so no further harm caused.
Patient Sequence No: 1, Text Type: N, H10


[181763920] The customer reports that the tip of the ptd thrombectomy device broke off and became lodged within the soft tissue just below the elbow. Attempts to remove it were unsuccessful due to its extravascular location.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9680794-2020-00109
MDR Report Key9780052
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-03-03
Date of Report2020-02-10
Date of Event2020-02-06
Date Mfgr Received2020-03-30
Device Manufacturer Date2019-11-19
Date Added to Maude2020-03-03
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 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 KIT
Generic NameCATHETER, EMBOLECTOMY
Product CodeDXE
Date Received2020-03-03
Catalog NumberPT-65509-HFC
Lot Number13F19L0323
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerARROW INTERNATIONAL INC.
Manufacturer AddressREADING PA


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-03

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