CAROTID WALLSTENT 26605

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 2020-01-02 for CAROTID WALLSTENT 26605 manufactured by Boston Scientific Corporation.

Event Text Entries

[177347511] Age at the time of event: 18 years or older. (b)(6).
Patient Sequence No: 1, Text Type: N, H10


[177347512] It was reported that catheter became entrapped on the guidewire. 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 However, upon advancing, the device became stuck with the non-bsc wire and could not be withdrawn.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 Number2134265-2019-16123
MDR Report Key9538975
Report SourceCOMPANY REPRESENTATIVE,DISTRI
Date Received2020-01-02
Date of Report2020-02-28
Date of Event2019-12-13
Date Mfgr Received2020-02-12
Device Manufacturer Date2019-03-27
Date Added to Maude2020-01-02
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 StreetBALLYBRIT BUSINESS PARK
Manufacturer CityGALWAY
Manufacturer CountryEI
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCAROTID WALLSTENT
Generic NameSTENT, CAROTID
Product CodeNIM
Date Received2020-01-02
Returned To Mfg2020-01-07
Model Number26605
Catalog Number26605
Lot Number0023548420
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerBOSTON SCIENTIFIC CORPORATION
Manufacturer AddressTWO SCIMED PLACE MAPLE GROVE MN 55311 US 55311


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-02

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