NEUROFORM 3 EZ 2.5MM X 15MM - CE M003EN3E25150

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 2020-03-11 for NEUROFORM 3 EZ 2.5MM X 15MM - CE M003EN3E25150 manufactured by Stryker Neurovascular Cork.

Event Text Entries

[183295520] Device not received for evaluation yet.
Patient Sequence No: 1, Text Type: N, H10


[183295521] It was reported that during atherosclerosis stenosis procedure at basilar artery, resistance was experienced while advancing the subject stent inside the micro catheter shaft and upon removal, the subject stent was found prematurely detached. The stent was replaced and the procedure was completed successfully. There were no clinical consequences reported to the patient.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3008881809-2020-00062
MDR Report Key9820935
Report SourceHEALTH PROFESSIONAL
Date Received2020-03-11
Date of Report2020-03-11
Date of Event2019-05-08
Date Mfgr Received2020-02-20
Date Added to Maude2020-03-11
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 G1STRYKER NEUROVASCULAR CORK
Manufacturer StreetIDA INDUSTRIAL ESTATE MODEL FARM ROAD
Manufacturer CityCORK NA
Manufacturer CountryIE
Manufacturer Postal CodeNA
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameNEUROFORM 3 EZ 2.5MM X 15MM - CE
Generic NameSTENT, INTRACRANIAL NEUROVASCULAR
Product CodeNJE
Date Received2020-03-11
Catalog NumberM003EN3E25150
Lot Number20953409
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSTRYKER NEUROVASCULAR CORK
Manufacturer AddressIDA INDUSTRIAL ESTATE MODEL FARM ROAD CORK NA IE NA


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-11

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