WOLVERINE CORONARY CUTTING BALLOON 3855

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 2020-03-25 for WOLVERINE CORONARY CUTTING BALLOON 3855 manufactured by Boston Scientific Corporation.

Event Text Entries

[185025835] It was reported that shaft got broke. The 90% stenosed target lesion was located in the very tortuous and very calcified left main ostial left anterior descending artery. A 15mm x 3. 00mm wolverine coronary cutting balloon was selected for use. During the procedure, while advancing into the heart the hypo tube got kinked and eventually the shaft broke outside the tuohy. The device was simply removed by pulling it out and slid out easily. The procedure was completed with a different device. No complications were reported and patient did very well post procedure.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2134265-2020-03079
MDR Report Key9879208
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-03-25
Date of Report2020-03-25
Date of Event2020-03-03
Date Mfgr Received2020-03-03
Device Manufacturer Date2019-12-11
Date Added to Maude2020-03-25
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 IRELAND LIMITED
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
Generic NameCATHETER, PERCUTANEOUS TRANSLUMINAL CORONARY ANGIOPLASTY (PTCA), CUTTING/SCORING
Product CodeNWX
Date Received2020-03-25
Model Number3855
Catalog Number3855
Lot Number0024915392
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 2020-03-25

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.