BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MX-PRO R3 AMBULANCE COT

    MDR report key: 1941134 · Received December 8, 2010

    Report

    Report Number
    1831750-2010-04610
    Event Type
    Malfunction
    Date Received
    December 8, 2010
    Date of Event
    November 8, 2010
    Report Date
    November 8, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIVISION
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    OTHER HEIGHT ADJUSTMENT RACK.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE HEIGHT ADJUSTMENT RACKS BOWED. NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MX-PRO R3 AMBULANCE COT STRETCHER, WHEELED FPO STRYKER CORP., MEDICAL DIVISION 6082 NA

    Patients

    Seq Age Sex Outcome Treatment
    1