BEUDAMED
    FDA Recall Terminated

    Axiom Artis MP X-Ray System

    Recall: Z-0818-05 · Initiated April 1, 2005

    Recall

    Recall Number
    Z-0818-05
    Event Number
    31647
    Firm
    Siemens Medical Solutions USA, Inc
    FEI Number
    2240869
    Product Code
    IZI
    Status
    Terminated
    Root Cause
    Other
    Initiated
    April 1, 2005
    Posted
    May 11, 2005
    Terminated
    August 18, 2005
    Address
    51 Valley Stream Pkwy, Malvern, PA, 19355-1406

    Description

    Axiom Artis MP X-Ray System

    Reason

    potential problem with the fluoroscopy switch on the power grip

    Action

    The recalling firm''s Customer Service Engineers are visiting each account to correct/replace the Power Grip button.

    Distribution

    The products were shipped to hospitals in AL, AZ, DC, DE, IA, MI, NC, NE, PA, RI, TX, WA, and WI.

    Quantity

    21 units