BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MX-PRO R-3 AMBULANCE COT

    MDR report key: 4222798 · Received November 4, 2014

    Report

    Report Number
    0001831750-2014-03318
    Event Type
    Injury
    Date Received
    November 4, 2014
    Date of Event
    June 18, 2012
    Report Date
    October 10, 2014
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    FPO
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE DEVICE HAS NOT BEEN MADE AVAILABLE FOR EVALUATION.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE USER OF THIS DEVICE WAS INJURED REQUIRING MEDICAL INTERVENTION. FURTHER INFORMATION REGARDING THIS EVENT WAS NOT PROVIDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    707497 MX-PRO R-3 AMBULANCE COT STRETCHER, WHEELED FPO STRYKER MEDICAL-KALAMAZOO

    Patients

    Seq Age Sex Outcome Treatment
    1