BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CONICAL EXTRACTOR, MALE, LEFT HAND 3.5 MM

    MDR report key: 2251358 · Received August 10, 2011

    Report

    Report Number
    9610622-2011-00364
    Event Type
    Malfunction
    Date Received
    August 10, 2011
    Date of Event
    July 20, 2011
    Report Date
    July 20, 2011
    Manufacturer
    STRYKER OSTEOSYNTHESIS KIEL
    Product Code
    LXH
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    ADD'L INFO HAS BEEN REQUESTED. ONCE THE INVESTIGATION HAS BEEN COMPLETED ANY ADD'L INFO WILL BE REPORTED IN A SUPPLEMENTAL REPORT.

    Description of Event or Problem · 1

    IT WAS REPORTED, EXTRACTOR DOES NOT ENGAGE SCREW HEAD. SYNTHESE EXTRACTOR WORKED PERFECTLY. NON-STRYKER REVISION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CONICAL EXTRACTOR, MALE, LEFT HAND 3.5 MM INSTRUMENT LXH STRYKER OSTEOSYNTHESIS KIEL NA UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK Other