WOLVERINE CORONARY CUTTING BALLOON MONORAIL 3851

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 2020-03-26 for WOLVERINE CORONARY CUTTING BALLOON MONORAIL 3851 manufactured by Boston Scientific Corporation.

Event Text Entries

[185214960] Age at time of event: 18 years or older.
Patient Sequence No: 1, Text Type: N, H10


[185214961] It was reported that a shaft break occurred. A percutaneous coronary intervention was being performed. While advancing a 10mm x 3. 00mm wolverine coronary cutting balloon to the target lesion, the shaft broke sometime between the hemostasis valve and the stenosed lesion. The device was removed and the procedure was completed with another of the same device. There were no patient complications and the patient was reported to be fine following the procedure.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2134265-2020-03667
MDR Report Key9887042
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-03-26
Date of Report2020-03-26
Date of Event2019-12-18
Date Mfgr Received2020-03-11
Device Manufacturer Date2018-08-24
Date Added to Maude2020-03-26
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 ContactJAY JOHNSON
Manufacturer StreetTWO SCIMED PLACE
Manufacturer CityMAPLE GROVE MN 55311
Manufacturer CountryUS
Manufacturer Postal55311
Manufacturer Phone7634942574
Manufacturer G1BOSTON SCIENTIFIC CORPORATION
Manufacturer StreetBALLYBRIT BUSINESS PARK
Manufacturer CityGALWAY
Manufacturer CountryEI
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameWOLVERINE CORONARY CUTTING BALLOON MONORAIL
Generic NameCATHETER, PERCUTANEOUS TRANSLUMINAL CORONARY ANGIOPLASTY (PTCA), CUTTING/SCORING
Product CodeNWX
Date Received2020-03-26
Returned To Mfg2020-03-23
Model Number3851
Catalog Number3851
Lot Number0022561173
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerBOSTON SCIENTIFIC CORPORATION
Manufacturer AddressTWO SCIMED PLACE MAPLE GROVE MN 55311 US 55311


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-26

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