FG GATEWAY OTW OUS 2.25MM X 15MM M0032072415220

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2018-06-26 for FG GATEWAY OTW OUS 2.25MM X 15MM M0032072415220 manufactured by Boston Scientific - Minn.

Event Text Entries

[112427112] It was reported that during a procedure to treat the left middle cerebral artery (mca) stenosis, the subject device balloon couldn? T be expanded. Therefore; the subject device was withdrawn from the patient? S body and the middle of the subject device was found to be leaked. The procedure was successfully completed with a new same type of the device without clinical consequences to the patient.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3008853977-2018-00029
MDR Report Key7640062
Report SourceHEALTH PROFESSIONAL
Date Received2018-06-26
Date of Report2018-08-10
Date of Event2018-05-30
Date Mfgr Received2018-07-17
Device Manufacturer Date2016-01-05
Date Added to Maude2018-06-26
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 ContactMR. TARA LOPEZ
Manufacturer Street47900 BAYSIDE PARKWAY
Manufacturer CityFREMONT CA 94538
Manufacturer CountryUS
Manufacturer Postal94538
Manufacturer Phone5104132500
Manufacturer G1BOSTON SCIENTIFIC - MINN
Manufacturer StreetONE 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 NameFG GATEWAY OTW OUS 2.25MM X 15MM
Generic NameCATHETER, BALLOON TYPE
Product CodeGBA
Date Received2018-06-26
Returned To Mfg2018-06-15
Catalog NumberM0032072415220
Lot Number19664066
Device Expiration Date2018-12-31
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerBOSTON SCIENTIFIC - MINN
Manufacturer AddressONE SCIMED PLACE MAPLE GROVE MN 55311 US 55311


Patients

Patient NumberTreatmentOutcomeDate
10 2018-06-26

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