BEUDAMED
    FDA Recall Terminated

    Cerner Bridge Medical Transfusion Administration and Specimen Collections, Versions 3.4.0, 3.4.1 and 3.4.2.

    Recall: Z-1236-2009 · Initiated January 19, 2009

    Recall

    Recall Number
    Z-1236-2009
    Event Number
    51319
    Firm
    Cerner Corp
    FEI Number
    1931259
    Product Code
    JQP
    Status
    Terminated
    Root Cause
    Software design
    Initiated
    January 19, 2009
    Posted
    May 1, 2009
    Terminated
    March 22, 2012
    Address
    2800 Rockcreek Pkwy, Kansas City, MO, 64117-2521

    Description

    Cerner Bridge Medical Transfusion Administration and Specimen Collections, Versions 3.4.0, 3.4.1 and 3.4.2.

    Reason

    Specimen labels printing incorrect patient demographics.

    Action

    Cerner Corporation issued a "Priority Review Flash" dated January 15, 2009 via e-mail to consignees using the software. The letter described the violative nature of the software and explained the proper navigation controls needed to prevent further issues. Further questions should be addressed to Bridge Client Support at 1-800-786-0239.

    Distribution

    Nationwide distribution to states of OH, NC, MO and MI.

    Quantity

    4