BEUDAMED
    FDA Adverse Event Other Summary report: N

    MAXISLIDE

    MDR report key: 308637 · Received December 13, 2000

    Report

    Report Number
    9617021-2000-00222
    Event Type
    Other
    Date Received
    December 13, 2000
    Date of Event
    November 13, 2000
    Report Date
    December 13, 2000
    Manufacturer
    ARJO, LTD.
    Product Code
    KME
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    THE FACILITY REPORTS WHILE THE PT WAS UNDER ANESTHESIA, THE OPERATING TABLE WAS POSITIONED IN THE HEAD-DOWN POSITION. IN THIS POSITION, THE PT SLID DOWN THE TABLE AND WAS PREVENTED FROM FALLING OFF THE OPERATING TABLE BY THE ANESTHESIOLOGIST'S EQUIPMENT AND PHYSICAL RESTRAINT BY MEMBERS OF THE STAFF. NO INJURIES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MAXISLIDE SLIDING SHEET KME ARJO, LTD. NSAXXXX NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other