JETSTREAM XC ATHERECTOMY CATHETER 45007

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-03-06 for JETSTREAM XC ATHERECTOMY CATHETER 45007 manufactured by Boston Scientific Corporation.

Event Text Entries

[182428687] It was reported that the device became entrapped on the guidewire a 2. 4mm jetstream xc atherectomy catheter and a non-bsc guidewire were selected for use in the superficial femoral artery (sfa). During the procedure, the device was activated for around 4 minutes and then the device became entrapped on the wire. The catheter and guidewire were removed together as one unit. The procedure was completed by dilation only without further atherectomy. There were no patient complications and the patient was stable post procedure.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2134265-2020-02641
MDR Report Key9800114
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-03-06
Date of Report2020-03-06
Date of Event2020-02-26
Date Mfgr Received2020-02-27
Device Manufacturer Date2019-12-04
Date Added to Maude2020-03-06
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 ContactJAY JOHNSON
Manufacturer StreetTWO SCIMED PLACE
Manufacturer CityMAPLE GROVE MN 55311
Manufacturer CountryUS
Manufacturer Postal55311
Manufacturer Phone7634942574
Manufacturer G1BOSTON SCIENTIFIC CORK LIMITED
Manufacturer StreetMODEL FARM ROAD
Manufacturer CityCORK
Manufacturer CountryEI
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameJETSTREAM XC ATHERECTOMY CATHETER
Generic NameCATHETER, PERIPHERAL, ATHERECTOMY
Product CodeMCW
Date Received2020-03-06
Model Number45007
Catalog Number45007
Lot Number0024871077
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBOSTON SCIENTIFIC CORPORATION
Manufacturer AddressTWO SCIMED PLACE MAPLE GROVE MN 55311 US 55311


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-06

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