RENEGADE HI-FLO 29420

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 2020-03-11 for RENEGADE HI-FLO 29420 manufactured by Boston Scientific Corporation.

Event Text Entries

[183099040] It was reported that the catheter split apart. A 135/10 renegade hi-flo catheter infusion was selected for use in a transarterial chemoembolization (tace) procedure. During the procedure, after beads were injected through the catheter, it was noted that the device split apart and was connected only by a protective cover. The device was removed by pulling everything out since the catheter was still inside the larger catheter. Nothing remained inside the patient's body. The vessel was rewired and the procedure was completed with another of the same device. No patient complications were reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2134265-2020-02867
MDR Report Key9820526
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-03-11
Date of Report2020-03-11
Date of Event2020-02-14
Date Mfgr Received2020-02-28
Device Manufacturer Date2019-08-02
Date Added to Maude2020-03-11
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 NameRENEGADE HI-FLO
Generic NameCATHETER, CONTINUOUS FLUSH
Product CodeKRA
Date Received2020-03-11
Model Number29420
Catalog Number29420
Lot Number0024206434
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 2020-03-11

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