OCCLUDER M0062201070 220107

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 2019-01-08 for OCCLUDER M0062201070 220107 manufactured by Boston Scientific Corporation.

Event Text Entries

[132351492] (b)(4). According to the complainant, the suspect device has been disposed and is not available for return. If any further relevant information is received, a supplemental mdr will be filed.
Patient Sequence No: 1, Text Type: N, H10


[132351493] It was reported to boston scientific corporation that an occluder balloon catheter was used along with a gemini retrieval basket in the kidney during a percutaneous nephrolithonomy (pcnl) procedure performed on (b)(6) 2018. According to the complainant, during the procedure, the balloon burst. The procedure was completed with another occluder balloon catheter.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3005099803-2018-62435
MDR Report Key8225993
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-01-08
Date of Report2019-01-08
Date of Event2018-12-07
Date Mfgr Received2018-12-12
Device Manufacturer Date2017-10-09
Date Added to Maude2019-01-08
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 CORK LIMITED
Manufacturer StreetCORK BUSINESS TECHNOLOGY PARK MODEL FARM ROAD
Manufacturer CityCORK
Manufacturer CountryEI
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameOCCLUDER
Generic NameCATHETER, UROLOGICAL
Product CodeEYB
Date Received2019-01-08
Model NumberM0062201070
Catalog Number220107
Lot Number0021231455
Device Expiration Date2019-03-11
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBOSTON SCIENTIFIC CORPORATION
Manufacturer Address300 BOSTON SCIENTIFIC WAY MARLBOROUGH MA 01752 US 01752


Patients

Patient NumberTreatmentOutcomeDate
10 2019-01-08

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