MICROPLEX VFC FILL COIL VFC030610-V-A

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 2017-05-16 for MICROPLEX VFC FILL COIL VFC030610-V-A manufactured by Microvention, Inc..

Event Text Entries

[75325447] The lot number was provided. A review of the approved device history records indicated the lot met all release criteria. A lot history trending review was performed and there were no similar complaints for this lot number. The device has not yet been returned for evaluation. The investigation is currently underway. The device was used during the same procedure as was reported in mfr. Report# 2032493-2017-00116.
Patient Sequence No: 1, Text Type: N, H10


[75325448] It was reported that while repositioning an embolization coil in a ruptured aneurysm, the coil stretched and then detached in the microcatheter. Both segments of the coil were removed together with the microcatheter from the patient. There was no reported patient injury. The patient's current status is reported to be good.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2032493-2017-00117
MDR Report Key6571489
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2017-05-16
Date of Report2017-04-17
Date of Event2017-04-17
Date Mfgr Received2017-04-17
Device Manufacturer Date2015-12-02
Date Added to Maude2017-05-16
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 ContactMS. DEBBY CALLAHAN
Manufacturer Street1311 VALENCIA AVENUE
Manufacturer CityTUSTIN CA 92780
Manufacturer CountryUS
Manufacturer Postal92780
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMICROPLEX VFC FILL COIL
Generic NameEMBOLIZATION COIL
Product CodeHGC
Date Received2017-05-16
Model NumberVFC030610-V-A
Lot Number151202VC2
OperatorPHYSICIAN
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerMICROVENTION, INC.
Manufacturer Address1311 VALENCIA AVENUE TUSTIN CA 92780 US 92780


Patients

Patient NumberTreatmentOutcomeDate
10 2017-05-16

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