BEUDAMED
    FDA Adverse Event Injury Summary report: N

    STRYKER CORPORATION

    MDR report key: 1515926 · Received October 21, 2009

    Report

    Report Number
    MW5013167
    Event Type
    Injury
    Date Received
    October 21, 2009
    Date of Event
    December 13, 2000
    Report Date
    October 21, 2009
    Product Code
    MEB
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    UT, US
    Reporter Occupation
    ATTORNEY

    Narratives

    Description of Event or Problem · 1

    USE OF POSTOPERATIVE PAIN PUMP DESTROYED SHOULDER CARTILAGE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 STRYKER CORPORATION PAIN-PUMP SHOULDER MEB

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention