BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MIS 4:1 IMPACTOR/EXTRACTOR

    MDR report key: 1853796 · Received September 29, 2010

    Report

    Report Number
    2249697-2010-01290
    Event Type
    Malfunction
    Date Received
    September 29, 2010
    Date of Event
    September 9, 2010
    Report Date
    September 9, 2010
    Manufacturer
    STRYKER ORTHOPAEDICS MAHWAH
    Product Code
    LXH
    PMA / PMN Number
    NA
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    A SUPPLEMENTAL REPORT WILL BE SUBMITTED UPON COMPLETION OF THE INVESTIGATION.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT: "NOTICED THAT THE TRIGGER KEEPS FALLING OUT. NO PATIENT CONSEQUENCES."

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MIS 4:1 IMPACTOR/EXTRACTOR INSTRUMENT LXH STRYKER ORTHOPAEDICS MAHWAH NA SBZW07

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK Other