WALLFLEX DUODENAL M00565010 6501

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 2018-11-19 for WALLFLEX DUODENAL M00565010 6501 manufactured by Boston Scientific Corporation.

Event Text Entries

[127858952] (b)(4). The device has not been received for analysis. Upon receipt and completion of the failure analysis of the complaint device, if there is any further relevant information from that review, a supplemental medwatch will be filed.
Patient Sequence No: 1, Text Type: N, H10


[127858953] It was reported to boston scientific corporation on (b)(6) 2018 that a wallflex duodenal stent has been implanted to treat a malignant stricture in the duodenum during a procedure performed on (b)(6) 2018. Reportedly, the patient's anatomy was not dilated prior to stent placement. According to the complainant, during the procedure, the stent was intentionally released, but was deployed distally from the target location. Reportedly, the stent remains implanted and a different stent was placed proximally to cover the entire stricture. There were no patient complications reported as a result of this event.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3005099803-2018-61514
MDR Report Key8087162
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2018-11-19
Date of Report2019-01-24
Date of Event2018-11-02
Date Mfgr Received2018-12-01
Device Manufacturer Date2018-09-03
Date Added to Maude2018-11-19
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 ContactCAROLE MORLEY
Manufacturer Street300 BOSTON SCIENTIFIC WAY
Manufacturer CityMARLBOROUGH MA 01752
Manufacturer CountryUS
Manufacturer Postal01752
Manufacturer Phone5086834015
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 NameWALLFLEX DUODENAL
Generic NameSTENT,METALLIC,EXPANDABLE,DUODENAL
Product CodeMUM
Date Received2018-11-19
Returned To Mfg2018-11-16
Model NumberM00565010
Catalog Number6501
Lot Number0022597824
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerBOSTON SCIENTIFIC CORPORATION
Manufacturer Address300 BOSTON SCIENTIFIC WAY MARLBOROUGH MA 01752 US 01752


Patients

Patient NumberTreatmentOutcomeDate
10 2018-11-19

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