BEUDAMED
    FDA Adverse Event Other Summary report: N

    MX-PRO R-3 AMBULANCE COT

    MDR report key: 1406007 · Received June 18, 2009

    Report

    Report Number
    1831750-2009-00400
    Event Type
    Other
    Date Received
    June 18, 2009
    Date of Event
    May 22, 2009
    Report Date
    May 22, 2009
    Manufacturer
    STRYKER CORP. MEDICAL DIVISION
    Product Code
    FPO
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT A COT HAS DROPPED TWICE. ALLEGEDLY AN EMT SUSTAINED A STRAINED ELBOW BUT DID NOT REQUIRE ANY MEDICAL INTERVENTION. NO PT INJURIES WERE SUSTAINED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MX-PRO R-3 AMBULANCE COT AMBULANCE COT FPO STRYKER CORP. MEDICAL DIVISION 6082 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK