BEUDAMED
    FDA Adverse Event Other Summary report: N

    POLARUS CORTICAL SCREW

    MDR report key: 385601 · Received March 25, 2002

    Report

    Report Number
    3025141-2001-00003
    Event Type
    Other
    Date Received
    March 25, 2002
    Report Date
    March 23, 2002
    Manufacturer
    ACUMED, INC.
    Product Code
    HWC
    Removal / Correction Number
    Z-0277-2
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SW
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    EXPIRATION DATE ON STERILE PART# HCO-3250-S SHOULD BE PRINTED ON THE LABELING AS 2006-08 INSTEAD OF 2008-06.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 POLARUS CORTICAL SCREW IMPLANT HWC ACUMED, INC. * W02675

    Patients

    Seq Age Sex Outcome Treatment
    1 NA