BEUDAMED
    FDA Recall Terminated

    Zoll M Series Automated Defibrillator (AED)

    Recall: Z-1472-04 · Initiated August 2, 2004

    Recall

    Recall Number
    Z-1472-04
    Event Number
    29959
    Firm
    Zoll Medical Corporation
    FEI Number
    1220908
    Product Code
    MKT
    Status
    Terminated
    Root Cause
    Other
    Initiated
    August 2, 2004
    Posted
    September 17, 2004
    Terminated
    February 13, 2017
    Address
    269 Mill Rd, Chelmsford, MA, 01824-4105

    Description

    Zoll M Series Automated Defibrillator (AED)

    Reason

    Visual Sreen display and audible prompt may not advise to 'Press Shock'

    Action

    Zoll Medical notified consignees by letter on 8/2/04 via Certified Mail. Users are advised of the problem and the softtware upgrade.

    Distribution

    Nationwide

    Quantity

    5649 units