BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    M-1 COT

    MDR report key: 1800572 · Received August 3, 2010

    Report

    Report Number
    1831750-2010-01693
    Event Type
    Malfunction
    Date Received
    August 3, 2010
    Date of Event
    July 5, 2010
    Report Date
    July 6, 2010
    Manufacturer
    STRYKER CORP MEDICAL DIVISION
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AS
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE TREND TUBE WELDMENT BENT CORRECTLY INCORRECTLY PROHIBITING. BOTH GUIDES FROM FITTING INTO THEIR RESPECTIVE SLOTS, RENDERING TREND INOPERABLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 M-1 COT STRETCHER WHEELED FPO STRYKER CORP MEDICAL DIVISION 6100 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK