BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MX-PRO R-3 AMBULANCE COT

    MDR report key: 2141369 · Received June 1, 2011

    Report

    Report Number
    1831750-2011-05334
    Event Type
    Malfunction
    Date Received
    June 1, 2011
    Date of Event
    May 4, 2011
    Report Date
    May 4, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE SVC TECHNICIANS NOTES AND CONVERSATIONS FOUND THE CAUSE OF THE ALLEGED ISSUE AS TO WHY THE COT WAS DROPPING WHEN THE OPERATOR SQUEEZED THE RELEASE HANDLE WAS DUE TO THE CUSTOMER SQUEEZING THE RELEASE HANDLE WHILE PULLING UP ON THE COT SLIGHTLY DISENGAGING THE COT FROM THE HEIGHT ADJUSTMENT RACK. IT WAS FOUND THE OPERATOR WAS USING AN IMPROPER TECHNIQUE.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SVC REPORT THAT THE COT CAN DROP WHEN THE RELEASE HANDLE IS SQUEEZED AND NO WEIGHT WAS ON THE LITTER. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MX-PRO R-3 AMBULANCE COT STRETCHER, WHEELED FPO STRYKER MEDICAL 6082 NA

    Patients

    Seq Age Sex Outcome Treatment
    1