UROMAX ULTRA M0062251010 225-101

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 2019-04-30 for UROMAX ULTRA M0062251010 225-101 manufactured by Boston Scientific Corporation.

Event Text Entries

[143681548] Patient exact age is unknown; however it was reported that the patient was over the age of 18. (b)(6). (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


[143681549] It was reported to boston scientific corporation that a uromax ultra dilatation balloon was used in the kidney during a retrograde intrarenal surgery (rirs) procedure performed on (b)(6) 2019. According to the complainant, during preparation, it was noted that the balloon would not inflate due to a leak. The procedure was completed with a different device. There were no patient complications reported as a result of this event. The patient condition at the conclusion of the procedure was reported to be stable.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3005099803-2019-02216
MDR Report Key8566327
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-04-30
Date of Report2019-04-30
Date of Event2019-04-04
Date Mfgr Received2019-04-04
Device Manufacturer Date2018-06-25
Date Added to Maude2019-04-30
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 NameUROMAX ULTRA
Generic NameDILATOR, CATHETER, URETERAL
Product CodeKOE
Date Received2019-04-30
Model NumberM0062251010
Catalog Number225-101
Lot Number0022297400
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 2019-04-30

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