BEUDAMED
    FDA Recall Terminated

    KCI Underbed Inverter, Accessory to Powered Flotation Therapy Bed, manufactured by Kinetic Concepts, Inc., San Antonio, TX. Model number 201189

    Recall: Z-0890-04 · Initiated March 22, 2004

    Recall

    Recall Number
    Z-0890-04
    Event Number
    28683
    Firm
    Kinetic Concepts, Inc
    FEI Number
    1625774
    Product Code
    IOQ
    Status
    Terminated
    Root Cause
    Other
    Initiated
    March 22, 2004
    Posted
    July 20, 2004
    Terminated
    November 2, 2005
    Address
    4958 Stout Dr, San Antonio, TX, 78219-4334

    Description

    KCI Underbed Inverter, Accessory to Powered Flotation Therapy Bed, manufactured by Kinetic Concepts, Inc., San Antonio, TX. Model number 201189

    Reason

    Battery outgassing of powered hospital beds

    Action

    The firm initiated the recall via letter on 03/22/2004.

    Distribution

    Product was distributed domestically in the following states: IN, CA, NH, OR, PA, TX, WI, CO, IA, KS, MO, ID, MA, NC, IL, OH, MN, AZ, NE, HI, PR, NC

    Quantity

    33 units