BEUDAMED
    FDA Adverse Event Summary report: N

    3085 SURGICAL TABLE

    MDR report key: 4133148 · Received October 1, 2014

    Report

    Report Number
    1043572-2014-00099
    Date Received
    October 1, 2014
    Date of Event
    September 3, 2014
    Report Date
    October 1, 2014
    Manufacturer
    STERIS CORPORATION - MONTGOMERY
    Product Code
    FQO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VT, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    A STERIS SERVICE TECHNICIAN INSPECTED THE SURGICAL TABLE AND FOUND THAT THE FLOOR LOCK FEET REQUIRED ADJUSTMENT. THE FLOOR LOCK FEET WERE NOT MAKING CONTACT WITH THE FLOOR PROPERLY ALLOWING THE WHEELS TO REMAIN ON THE FLOOR. THE TECHNICIAN ADJUSTED THE FLOOR LOCK FEET, TESTED THE TABLE AND RETURNED IT TO SERVICE. NO ADDITIONAL ISSUES HAVE BEEN REPORTED.

    Description of Event or Problem · 1

    THE USER FACILITY REPORTED THAT WHILE A PATIENT WAS PRESENT ON THE TABLE, THE TABLE WOULD NOT LOCK. NO INJURIES OR PROCEDURAL DELAYS/CANCELLATIONS WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    611140 3085 SURGICAL TABLE SURGICAL TABLE FQO STERIS CORPORATION - MONTGOMERY

    Patients

    Seq Age Sex Outcome Treatment
    1