BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    RUGGED M1 AMBULANCE COT

    MDR report key: 1883049 · Received October 22, 2010

    Report

    Report Number
    1831750-2010-03141
    Event Type
    Malfunction
    Date Received
    October 22, 2010
    Date of Event
    September 29, 2010
    Report Date
    September 29, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    RESULTS: SLIDE TUBE CRACK.

    Description of Event or Problem · 1

    IT WAS REPORTED BY A CUSTOMER THAT THE CONNECTION PIECES OF THE SKID PIPE HAVE A FISSURE. NO ADVERSE CONSEQUENCES OR INJURIES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RUGGED M1 AMBULANCE COT STRETCHER, WHEELED FPO STRYKER CORP., MEDICAL DIV. 6100 NI

    Patients

    Seq Age Sex Outcome Treatment
    1