BEUDAMED
    FDA Enforcement Class II Ongoing

    HeartWare HVAD Pump Kit, REF 1104CA-CLIN

    Recall: Z-0747-2023 · Reported December 28, 2022

    Enforcement

    Recall Number
    Z-0747-2023
    Event ID
    91281
    Classification
    Class II
    Status
    Ongoing
    Product Type
    Devices
    Firm
    Heartware, Inc.
    Voluntary / Mandated
    Voluntary: Firm initiated
    Initial Notification
    Letter
    Report Date
    December 28, 2022
    Initiation Date
    November 29, 2022
    Classification Date
    December 21, 2022
    Address
    14400 Nw 60th Ave, Miami Lakes, FL, 33014-2807, United States

    Description

    HeartWare HVAD Pump Kit, REF 1104CA-CLIN

    Reason

    Over time, the driveline cover may become hardened, creating difficulty or an inability to slide the cover back to access the driveline to controller connector. Access to the driveline connector may be delayed, which may result in patient harm from a prolonged pump stop, if an urgent driveline connection or controller issue needs to be addressed. In the event a hardened driveline cover is observed, contact your Medtronic field representative for further assessment and/or servicing.

    Code Info

    Serial Numbers: HW24101, HW24102, HW24103, HW24104, HW24755, HW24763

    Distribution

    Worldwide distribution.

    Quantity

    6 units