BEUDAMED
    FDA Enforcement Class II Terminated

    ADVIA Centaur iPTH Calibrator 2 pk; REF 10492394. For in vitro diagnostic use in calibrating Intact PTH assays.

    Recall: Z-1514-2013 · Reported June 12, 2013

    Enforcement

    Recall Number
    Z-1514-2013
    Event ID
    65224
    Classification
    Class II
    Status
    Terminated
    Product Type
    Devices
    Firm
    Siemens Healthcare Diagnostics, Inc
    Voluntary / Mandated
    Voluntary: Firm initiated
    Initial Notification
    Letter
    Report Date
    June 12, 2013
    Initiation Date
    May 14, 2013
    Classification Date
    June 6, 2013
    Termination Date
    March 5, 2015
    Address
    333 Coney St, N/A, East Walpole, MA, 02032-1516, United States

    Description

    ADVIA Centaur iPTH Calibrator 2 pk; REF 10492394. For in vitro diagnostic use in calibrating Intact PTH assays.

    Reason

    iPTH Assay- reagent and calibrator lots may have demonstrated higher than anticipated variability

    Code Info

    Calibrator Lot Number: C5601 and C5602 Kit Lot Number/Exp. Date: 61405A01 27 Oct 2011 66517A02 27 Oct 2011 66611A02 27 Oct 2011 71997C02 27 Oct 2011

    Distribution

    Nationwide Distribution.

    Quantity

    99 (2 pk)