BEUDAMED
    FDA Enforcement Class II Ongoing

    Percuflex Plus Ureteral Stent Set 6FX26CM with .038 Sensor UPN: M006175263110

    Recall: Z-1734-2020 · Reported April 29, 2020

    Enforcement

    Recall Number
    Z-1734-2020
    Event ID
    85227
    Classification
    Class II
    Status
    Ongoing
    Product Type
    Devices
    Firm
    Boston Scientific
    Voluntary / Mandated
    Voluntary: Firm initiated
    Initial Notification
    Letter
    Report Date
    April 29, 2020
    Initiation Date
    March 9, 2020
    Classification Date
    April 17, 2020
    Address
    100 Boston Scientific Way, N/A, Marlborough, MA, 01752-1234, United States

    Description

    Percuflex Plus Ureteral Stent Set 6FX26CM with .038 Sensor UPN: M006175263110

    Reason

    An increase in the rate of complaints for difficulty or inability to track over the guidewire, may result in a procedural delay due to the need to exchange the affected device

    Code Info

    Lot Number: 24835477 (edited 1/13/2021)

    Distribution

    Nationwide Foreign: Europe, Middle East and Africa, the Americas (North America and South America, Asia Pacific and Japan

    Quantity

    32