BEUDAMED
    FDA Enforcement Class II Ongoing

    MEDLINE ELECTRIC SURGICAL CLIPPER AND BASE, REF DYND70800 Product Usage: Medline Surgical Clipper is intended for the removal of body hair from the patient as required prior to surgery or other minor procedures.

    Recall: Z-2756-2019 · Reported October 2, 2019

    Enforcement

    Recall Number
    Z-2756-2019
    Event ID
    83740
    Classification
    Class II
    Status
    Ongoing
    Product Type
    Devices
    Firm
    Medline Industries Inc
    Voluntary / Mandated
    Voluntary: Firm initiated
    Initial Notification
    Letter
    Report Date
    October 2, 2019
    Initiation Date
    September 6, 2019
    Classification Date
    September 26, 2019
    Address
    Three Lakes Drive, Northfield, IL, 60093, United States

    Description

    MEDLINE ELECTRIC SURGICAL CLIPPER AND BASE, REF DYND70800 Product Usage: Medline Surgical Clipper is intended for the removal of body hair from the patient as required prior to surgery or other minor procedures.

    Reason

    The recall is being conducted due to a potential defective component on the circuit board causing the charger base to overheat which could result in a charger base malfunction.

    Code Info

    14G1

    Distribution

    US Nationwide Distribution

    Quantity

    500 units