BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PRIME BIG WHEEL STRETCHER

    MDR report key: 3893765 · Received June 25, 2014

    Report

    Report Number
    0001831750-2014-03110
    Event Type
    Injury
    Date Received
    June 25, 2014
    Date of Event
    June 1, 2014
    Report Date
    June 2, 2014
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    FPO
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA
    Reporter Occupation
    NURSE

    Narratives

    Additional Manufacturer Narrative · 1

    IT WAS REPORTED THAT A VISITOR TRIPPED OVER THE CASTER AT THE FOOT END OF THE STRETCHER. AS A RESULT TO THE TRIPPING EVENT, IT WAS REPORTED THAT ALLEGEDLY THE VISITOR INJURED THEIR ANKLE WHICH WAS TREATED WITH AN ICE PACK ON THE ANKLE. THE CUSTOMER REPORTED THAT THERE WAS NO MALFUNCTIONS WITH THE PRODUCT AND REPORTED THAT THE LIKELY CAUSE AS TO WHY THE ALLEGED EVENT OCCURRED MAY HAVE BEEN DUE TO THE VISITOR NOT NOTICING THE WHEEL WHILE PASSING BY.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT A VISITOR AT THE USER FACILITY TRIPPED OVER THE CASTER WHEEL AT THE FOOT OF THE STRETCHER AND INJURED THEIR ANKLE AS A RESULT. FURTHER INFORMATION ON THE TREATMENT AND THE TYPE OF THE INJURY IS UNKNOWN AT THIS TIME.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT A VISITOR AT THE USER FACILITY TRIPPED OVER THE CASTER WHEEL AT THE FOOT OF THE STRETCHER AND INJURED THEIR ANKLE AS A RESULT. FURTHER INFORMATION ON THE TREATMENT AND THE TYPE OF THE INJURY IS UNKNOWN AT THIS TIME.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    370068 PRIME BIG WHEEL STRETCHER STRETCHER, WHEELED FPO STRYKER MEDICAL-KALAMAZOO

    Patients

    Seq Age Sex Outcome Treatment
    1