BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    STAIR PRO - MODEL 6252

    MDR report key: 1853036 · Received September 21, 2010

    Report

    Report Number
    1831750-2010-02483
    Event Type
    Malfunction
    Date Received
    September 21, 2010
    Date of Event
    July 19, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    RESTRAINT STRAP. IF ADDITIONAL INFORMATION FOUND TO BE RELEVANT BY THE MANUFACTURER IS DISCOVERED UPON INVESTIGATION, A FOLLOW-UP MDR WILL BE SUBMITTED.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THE ONE RESTRAINT STRAP IS BROKEN ON THE UNIT. IT IS FURTHER REPORTED THAT THERE WAS NO ADVERSE CONSEQUENCES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 STAIR PRO - MODEL 6252 STRETCHER HAND - CARRIED FPO STRYKER CORP., MEDICAL DIV. 6252 NA

    Patients

    Seq Age Sex Outcome Treatment
    1