BEUDAMED
    FDA Recall Terminated

    The product is a mobile 3-wheeled electric scooter, model HMV 220. The product contains either a red or blue base. The red base is identified with SKU #9153641905. The blue base is identified with SKU #9153641906. The product is distributed by the Invacare Corporation.

    Recall: Z-0521-06 · Initiated November 1, 2005

    Recall

    Recall Number
    Z-0521-06
    Event Number
    34405
    Firm
    Tung Keng Enterprise Co., Ltd. No.1, Lane 160, Section 2, Tan-Fu Road Tai-Tzu Hsiang, Taichung County Taiwan
    FEI Number
    3002667030
    Product Code
    INI
    Status
    Terminated
    Root Cause
    Other
    Initiated
    November 1, 2005
    Posted
    February 16, 2006
    Terminated
    May 8, 2012

    Description

    The product is a mobile 3-wheeled electric scooter, model HMV 220. The product contains either a red or blue base. The red base is identified with SKU #9153641905. The blue base is identified with SKU #9153641906. The product is distributed by the Invacare Corporation.

    Reason

    The throttle spring, located in the hand throttle assembly, can fracture, resulting in the scooter not stopping when the user releases the throttle.

    Action

    The recalling firm sent field correction instructions to their customers on or about 11/1/05.

    Distribution

    The product was distributed to OHL/Invacare, Rancho Technology Park Bldg. B 8950, Rancho Cucamonga, CA 91730; OHL/Invacare, 1100 Whitaker Road, Plainfield, IN 46168; Invacare Corporation, 39400 Taylor Parkway North Ridgeville, OH 44039; and Invacare, Dallas Texas Distribution Center, 3460 South Watson Rd., Arlington, TX 76014.

    Quantity

    8,213 total devices