FILTERWIRE EZ 44150

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,distri report with the FDA on 2020-02-28 for FILTERWIRE EZ 44150 manufactured by Boston Scientific Corporation.

Event Text Entries

[181602236] Age at time of event: 18 years or older. Initial reporter address: (b)(6).
Patient Sequence No: 1, Text Type: N, H10


[181602237] It was reported that catheter entrapment on wire occurred. The target lesion was located in the carotid artery. A 10. 0-31 carotid wallstent was advanced to treat the lesion. However, upon advancing, the device became stuck with the 190 cm mt filterwire ez and could not be withdrawn. The procedure was completed with another of the same device. No patient complications were reported and the patient's status was stable.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2134265-2020-02237
MDR Report Key9769561
Report SourceCOMPANY REPRESENTATIVE,DISTRI
Date Received2020-02-28
Date of Report2020-02-28
Date of Event2019-12-13
Date Mfgr Received2020-02-12
Device Manufacturer Date2019-06-12
Date Added to Maude2020-02-28
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 ContactJAY JOHNSON
Manufacturer StreetTWO SCIMED PLACE
Manufacturer CityMAPLE GROVE MN 55311
Manufacturer CountryUS
Manufacturer Postal55311
Manufacturer Phone7634942574
Manufacturer G1BOSTON SCIENTIFIC CORPORATION
Manufacturer Street2546 CALLE PRIMERA
Manufacturer CityALAJUELA
Manufacturer CountryCS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameFILTERWIRE EZ
Generic NameTEMPORARY CORONARY SAPHENOUS VEIN BYPASS GRAFT FOR EMBOLIC PROTECTION
Product CodeNFA
Date Received2020-02-28
Model Number44150
Catalog Number44150
Lot Number0023943268
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBOSTON SCIENTIFIC CORPORATION
Manufacturer AddressTWO SCIMED PLACE MAPLE GROVE MN 55311 US 55311


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-28

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