BEUDAMED
    FDA Recall Terminated

    AC Power Cords, 110V Manufactured by Electri-Cord Manufacturing Company in Westfield, PA. Power Cord #4100079 used with Kinair IV Model 22600, Kinair IV 60601 Model 216050, Triadyne Proventa Model 406000, Therapulse ATP/II Models 227800 and 227080.S, Kinair Medsurg Model 201001W, and Kinair Medsurg Pulse Model 40900.

    Recall: Z-0662-2010 · Initiated November 4, 2009

    Recall

    Recall Number
    Z-0662-2010
    Event Number
    53802
    Firm
    KCI USA, Inc.
    FEI Number
    1625774
    Product Code
    IOQ
    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 #4100079 used with Kinair IV Model 22600, Kinair IV 60601 Model 216050, Triadyne Proventa Model 406000, Therapulse ATP/II Models 227800 and 227080.S, Kinair Medsurg Model 201001W, and Kinair Medsurg Pulse Model 40900.

    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

    4,637 units