BEUDAMED
    FDA Recall Terminated

    RotoProne powered patient rotation bed, part #209500, distributed by Kinetic Concepts, Inc., San Antonio, TX.

    Recall: Z-0520-06 · Initiated January 24, 2005

    Recall

    Recall Number
    Z-0520-06
    Event Number
    34296
    Firm
    Kinetic Concepts, Inc
    FEI Number
    1625774
    Product Code
    IKZ
    Status
    Terminated
    Root Cause
    Other
    Initiated
    January 24, 2005
    Posted
    February 14, 2006
    Terminated
    June 29, 2006
    Address
    4958 Stout Dr, San Antonio, TX, 78219-4334

    Description

    RotoProne powered patient rotation bed, part #209500, distributed by Kinetic Concepts, Inc., San Antonio, TX.

    Reason

    To correct software issues in software versions 1.3 and 1.5 and to upgrade hatch latch handles to a more ergonomic design.

    Action

    All KCI Service Centers notified via Technical Bulletin of upgrades. 1/24/2005

    Distribution

    Devices distributed nationwide.

    Quantity

    91