ARROW ARROW(R) VPS(R) ACCESS KIT ASK-04001-DU9

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,user f report with the FDA on 2020-02-26 for ARROW ARROW(R) VPS(R) ACCESS KIT ASK-04001-DU9 manufactured by Arrow International Inc..

Event Text Entries

[184459089] (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[184459090] The customer states during insertion of the glide thru sheath, crumples and they must grab another sheath to start insertion.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1036844-2020-00066
MDR Report Key9757750
Report SourceCOMPANY REPRESENTATIVE,USER F
Date Received2020-02-26
Date of Report2020-02-07
Date of Event2020-01-27
Date Mfgr Received2020-03-19
Device Manufacturer Date2019-10-22
Date Added to Maude2020-02-26
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 INC.
Manufacturer Street312 COMMERCE PLACE
Manufacturer CityASHEBORO NC 27203
Manufacturer CountryUS
Manufacturer Postal Code27203
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameARROW ARROW(R) VPS(R) ACCESS KIT
Generic NameCATHETER, ULTRASOUND, INTRAVA
Product CodeOBJ
Date Received2020-02-26
Catalog NumberASK-04001-DU9
Lot Number23F19K0332
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 2020-02-26

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