BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MX-PRO R-3 AMBULANCE COT

    MDR report key: 3162287 · Received June 11, 2013

    Report

    Report Number
    0001831750-2013-05271
    Event Type
    Injury
    Date Received
    June 11, 2013
    Date of Event
    May 14, 2013
    Report Date
    May 15, 2013
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    FPO
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    IT WAS INCORRECTLY REPORTED THAT THE COT DROPPED. IT WAS FOUND DURING INVESTIGATION THAT THE COT LEGS WOULD NOT LOCK INTO POSITION. THE EMT STRAINED THEIR SHOULDER DURING THE INCIDENT BUT MEDICAL INTERVENTION COULD NOT BE CONFIRMED. THERE WAS PATIENT INVOLVEMENT; HOWEVER, NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

    Description of Event or Problem · 1

    IT WAS REPORTED COT DROPPED DURING PATIENT USE. THE EMT STRAINED THEIR SHOULDER DURING THE INCIDENT. THERE WAS PATIENT INVOLVEMENT; HOWEVER, NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE COT LEGS WOULD NOT LOCK INTO POSITION. THE EMT STRAINED THEIR SHOULDER DURING THE INCIDENT BUT MEDICAL INTERVENTION COULD NOT BE CONFIRMED. THERE WAS PATIENT INVOLVEMENT; HOWEVER, NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    262297 MX-PRO R-3 AMBULANCE COT STRETCHER, WHEELED FPO STRYKER MEDICAL-KALAMAZOO

    Patients

    Seq Age Sex Outcome Treatment
    1