BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    RITTER

    MDR report key: 2142585 · Received June 21, 2011

    Report

    Report Number
    1523530-2011-00017
    Event Type
    Malfunction
    Date Received
    June 21, 2011
    Date of Event
    May 26, 2011
    Report Date
    June 20, 2011
    Manufacturer
    MIDMARK CORP.
    Product Code
    GBB
    PMA / PMN Number
    EXEMPT
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Description of Event or Problem · 1

    A PT WAS PUNCTURED BY A STAPLE IN THE TABLE'S FOOTREST.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RITTER CHAIR, SURGICAL, AC-POWERED GBB MIDMARK CORP. 230-004

    Patients

    Seq Age Sex Outcome Treatment
    1