PASSPORT M0062181100 218-110

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 2019-05-21 for PASSPORT M0062181100 218-110 manufactured by Boston Scientific Corporation.

Event Text Entries

[145633755] (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 mdr will be filed.
Patient Sequence No: 1, Text Type: N, H10


[145633756] This report pertains to one of two passport balloon dilatation catheters used during the same procedure. It was reported to boston scientific corporation that two passport balloon dilatation catheter devices were used in the ureter duing a ureteroscopic lithotripsy (ursl) procedure performed on (b)(6) 2019. According to the complainant, during the procedure, the balloon burst. The same issue occured on the second passport balloon dilatation catheter. The procedure was completed with another passport balloon dilatation catheter. There were no patient complications reported as a result of this event.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3005099803-2019-02582
MDR Report Key8627570
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-05-21
Date of Report2019-08-13
Date of Event2019-04-29
Date Mfgr Received2019-07-18
Device Manufacturer Date2018-07-17
Date Added to Maude2019-05-21
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 NamePASSPORT
Generic NameDILATOR, CATHETER, URETERAL
Product CodeEZN
Date Received2019-05-21
Returned To Mfg2019-06-24
Model NumberM0062181100
Catalog Number218-110
Lot Number0022386813
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 2019-05-21

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