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 2019-05-24 for EXPRESS SD RENAL/BILIARY 20188 manufactured by Boston Scientific Corporation.

Event Text Entries

[146063809] It was reported that the stent dislodged. The 60-70% stenosed target lesion was located in a celiac artery. A 6. 0mmx14mmx150cm express sd stent was advanced for treatment using a 7fr im guide catheter and a. 018 guidewire. However, during procedure, it failed to cross the lesion. The physician attempted to pull the stent back into the guide catheter, but it would not go back. It was then attempted to remove the whole system but the stent came off of the balloon. A snare was used to remove the stent. The procedure was completed with a non-bsc device. No patient complications were reported and the patient was fine.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2134265-2019-05720
MDR Report Key8640258
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2019-05-24
Date of Report2019-05-24
Date of Event2016-11-11
Date Mfgr Received2019-05-10
Device Manufacturer Date2016-04-22
Date Added to Maude2019-05-24
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 ContactSONALI ARANGIL
Manufacturer StreetTWO SCIMED PLACE
Manufacturer CityMAPLE GROVE MN 55311
Manufacturer CountryUS
Manufacturer Postal55311
Manufacturer Phone6515827403
Manufacturer G1BOSTON SCIENTIFIC SCIMED, INC
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 Received2019-05-24
Model Number20188
Catalog Number20188
Lot Number0019179065
Device Expiration Date2019-04-30
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 2019-05-24

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