PERCUFLEX NEPHROURETERAL STENT 35375

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 2020-03-13 for PERCUFLEX NEPHROURETERAL STENT 35375 manufactured by Boston Scientific Corporation.

Event Text Entries

[183329012] Date of event is an estimated date based off the aware date month as the exact event date was not reported.
Patient Sequence No: 1, Text Type: N, H10


[183329013] It was reported that the stent was fractured. A 10/24 percuflex nephroureteral stent was selected for use. It was noted that the device was bent/fractured during shipping. No patient complications were reported and there was no impact on patient health as affected catheter was not used during the actual procedure.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2134265-2020-03066
MDR Report Key9829708
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-03-13
Date of Report2020-03-13
Date of Event2020-02-01
Date Mfgr Received2020-02-26
Device Manufacturer Date2019-04-22
Date Added to Maude2020-03-13
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 ContactJAY JOHNSON
Manufacturer StreetTWO SCIMED PLACE
Manufacturer CityMAPLE GROVE MN 55311
Manufacturer CountryUS
Manufacturer Postal55311
Manufacturer Phone7634942574
Manufacturer G1BOSTON SCIENTIFIC DE COSTA RICA S.R.L.
Manufacturer Street2546 CALLE PRIMERA
Manufacturer CityALAJUELA
Manufacturer CountryCS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePERCUFLEX NEPHROURETERAL STENT
Generic NameTUBE, DRAINAGE, SUPRAPUBIC
Product CodeFAD
Date Received2020-03-13
Model Number35375
Catalog Number35375
Lot Number0023675351
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 2020-03-13

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