BEUDAMED
    FDA Recall Terminated

    Spectre brand AC wall adapter to be used with ProControl 2 or ProHand battery powered upper limb prosthesis.

    Recall: Z-0959-05 · Initiated February 1, 2005

    Recall

    Recall Number
    Z-0959-05
    Event Number
    32060
    Firm
    Motion Control, Inc.
    FEI Number
    3001237006
    Product Code
    IQZ
    Status
    Terminated
    Root Cause
    Other
    Initiated
    February 1, 2005
    Posted
    July 6, 2005
    Terminated
    October 7, 2008
    Address
    2401 S 1070 W, Ste B, Salt Lake City, UT, 84119

    Description

    Spectre brand AC wall adapter to be used with ProControl 2 or ProHand battery powered upper limb prosthesis.

    Reason

    Incorrect AC wall adapter was distributed with prostheses. Incorrect use of adapters could damage the battery and cause a potential fire hazard.

    Action

    Consignees were notified by phone and letter on 2/3/2005.

    Distribution

    CA, DC, FL, NJ, OH, PA, SC, TN, TX, and Puerto Rico. No military, government or foreign distribution.

    Quantity

    20 units