BEUDAMED
    FDA Recall Terminated

    Easypump L T 60-24 infusion pump

    Recall: Z-0585-06 · Initiated January 17, 2006

    Recall

    Recall Number
    Z-0585-06
    Event Number
    34494
    Firm
    I-Flow Corporation
    FEI Number
    3011270181
    Product Code
    MEB
    Status
    Terminated
    Root Cause
    Other
    Initiated
    January 17, 2006
    Posted
    March 7, 2006
    Terminated
    February 5, 2007
    Address
    20202 Windrow Dr, Lake Forest, CA, 92630-8152

    Description

    Easypump L T 60-24 infusion pump

    Reason

    The sterile pack may contain the wrong infusion pump inside.

    Action

    The affected customer has been notified with a Notification letter dated January 17, 2006 via e-mail of Recall Notification Letter, with follow-up confirmation e-mails.

    Distribution

    France only

    Quantity

    549