BEUDAMED
    FDA Recall Terminated

    DC Power Adapter for use with the LIFEPAK 12 defibrillator/monitor.

    Recall: Z-0971-04 · Initiated May 5, 2004

    Recall

    Recall Number
    Z-0971-04
    Event Number
    29027
    Firm
    Medtronic Physio Control Corp
    FEI Number
    3015876
    Product Code
    LDD
    Status
    Terminated
    Root Cause
    Other
    Initiated
    May 5, 2004
    Posted
    July 20, 2004
    Terminated
    January 6, 2005
    Address
    11811 Willows Rd NE, Redmond, WA, 98073

    Description

    DC Power Adapter for use with the LIFEPAK 12 defibrillator/monitor.

    Reason

    The DC Power Adapter may fail to charge LIFEPAK NiCd 2.4 AH batteries used with the LIFEPAK 12 defibrillator/monitor.

    Action

    On 5/5/04 the firm issued a letter to consignees advising of the problem and that a service representative will contact them regarding replacement of the DC Power Adapter.

    Distribution

    The firm distributed devices to medical facilities, fire departments (first responders).

    Quantity

    1689