EXPRESS SD RENAL/BILIARY 20188

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 2020-03-05 for EXPRESS SD RENAL/BILIARY 20188 manufactured by Boston Scientific Corporation.

Event Text Entries

[182388341] Date of event: used the 1st day of the month of the bsc aware date as no event date was provided.
Patient Sequence No: 1, Text Type: N, H10


[182388342] It was reported that stent dislodgement occurred. A 5. 0mmx19mmx90cm express sd renal/biliary stent was advanced for treatment. However, during the procedure the stent came off the balloon before it was deployed. The physician removed the stent with a retrieval device. No further patient complications were reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2134265-2020-02611
MDR Report Key9793760
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-03-05
Date of Report2020-03-05
Date of Event2020-02-01
Date Mfgr Received2020-02-19
Device Manufacturer Date2017-04-06
Date Added to Maude2020-03-05
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 CORPORATION
Manufacturer StreetTWO SCIMED PLACE
Manufacturer CityMAPLE GROVE MN 55311
Manufacturer CountryUS
Manufacturer Postal Code55311
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameEXPRESS SD RENAL/BILIARY
Generic NameCATHETER, BILIARY, DIAGNOSTIC
Product CodeNIN
Date Received2020-03-05
Model Number20188
Catalog Number20188
Lot Number0020496511
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. Other 2020-03-05

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