BEUDAMED
    FDA Recall Terminated

    AC Power Cords, 110V Manufactured by Electri-Cord Manufacturing Company in Westfield, PA. Power Cord #M4268840 used with First Step All-In-One Canadian French Models 227500-09 and 227500, First Step All-In-One English Model 227500, Therakair Visio Models M8259978 and M6257763 pump only, and Proficare - Canada Model M8259988

    Recall: Z-0664-2010 · Initiated November 4, 2009

    Recall

    Recall Number
    Z-0664-2010
    Event Number
    53802
    Firm
    KCI USA, Inc.
    FEI Number
    1625774
    Product Code
    IKY
    Status
    Terminated
    Root Cause
    Nonconforming Material/Component
    Initiated
    November 4, 2009
    Posted
    January 25, 2010
    Terminated
    January 21, 2011
    Address
    4958 Stout Dr, San Antonio, TX, 78219-4334

    Description

    AC Power Cords, 110V Manufactured by Electri-Cord Manufacturing Company in Westfield, PA. Power Cord #M4268840 used with First Step All-In-One Canadian French Models 227500-09 and 227500, First Step All-In-One English Model 227500, Therakair Visio Models M8259978 and M6257763 pump only, and Proficare - Canada Model M8259988

    Reason

    Power cords may crack and fail inside plug with potential for fire hazard.

    Action

    Kinetics Concepts, Inc. (KCI) issued an "Urgent Medical Device Correction" letter dated November 4, 2009. Consignees were informed of the affected product and instructed to take necessary action to avoid any further issues associated with the product. For further information, contact KCI's technical support team at 1-800-275-4524 option #3.

    Distribution

    Nationwide and Canada

    Quantity

    1,384