WALLSTENT ENDOPROSTHESIS 26280

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,distri report with the FDA on 2020-03-03 for WALLSTENT ENDOPROSTHESIS 26280 manufactured by Boston Scientific Corporation.

Event Text Entries

[181839036] Age at time of event: 18 years or older.
Patient Sequence No: 1, Text Type: N, H10


[181839037] It was reported that stent did not fully expand post deployment. The target lesion was located in the iliac vein. A 14x40/9fr uni plus 75cm wallstent endoprosthesis was advanced for treatment. However, after deployment, the stent head was found not fully opened or the proximal end was still closed. The physician deployed a non-bsc stent to support the original one and the procedure was completed. No patient complications were reported and the patient's status was stable.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2134265-2020-02470
MDR Report Key9780153
Report SourceCOMPANY REPRESENTATIVE,DISTRI
Date Received2020-03-03
Date of Report2020-03-03
Date of Event2020-02-07
Date Mfgr Received2020-02-23
Device Manufacturer Date2019-08-26
Date Added to Maude2020-03-03
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 NameWALLSTENT ENDOPROSTHESIS
Generic NameCATHETER, BILIARY, DIAGNOSTIC
Product CodeMAF
Date Received2020-03-03
Model Number26280
Catalog Number26280
Lot Number0024326255
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
101. Required No Informationntervention 2020-03-03

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