BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ACCLAIM LINKED ULNAR METAL TRL

    MDR report key: 477553 · Received August 13, 2003

    Report

    Report Number
    1818910-2003-00589
    Event Type
    Injury
    Date Received
    August 13, 2003
    Date of Event
    July 16, 2003
    Report Date
    July 16, 2003
    Manufacturer
    DEPUY ORTHOPAEDICS, INC.
    Product Code
    LXH
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IN, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE CUSTOMER RETURNED A 1722-60-000 IN THE SLOT FOR THE 2722-60-000.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ACCLAIM LINKED ULNAR METAL TRL TOTAL HIP REPLACEMENT LXH DEPUY ORTHOPAEDICS, INC. NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other