BEUDAMED
    FDA Adverse Event Injury Summary report: N

    RITTER

    MDR report key: 22639147 · Received July 28, 2025

    Report

    Report Number
    1523530-2025-00006
    Event Type
    Injury
    Date Received
    July 28, 2025
    Date of Event
    July 8, 2025
    Report Date
    July 28, 2025
    Manufacturer
    MIDMARK CORPORATION
    Product Code
    GBB
    UDI-DI
    00841709106002
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MA, US
    Reporter Occupation
    BIOMEDICAL ENGINEER
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    ON JULY 10, 2025, MIDMARK CORPORATION WAS NOTIFIED OF AN INSTANCE THAT OCCURRED ON OR AROUND ON (B)(6) 2025, IN WHICH CLEANING PERSONNEL WERE CLEANING A MODEL 224 EXAM TABLE. WHILE CLEANING THE TABLE, THE FOOT CONTROL WAS ACTIVATED AND THE TABLE DESCENDED ONTO THEIR FOOT. MIDMARK CORPORATION HAS MADE MULTIPLE ATTEMPTS FOR FURTHER INFORMATION OF THE CURRENT STATE OF THE TABLE AND ADDITIONAL DETAILS OF THIS INSTANCE, ALTHOUGH NO FURTHER DETAILS HAVE BEEN MADE AVAILABLE. SHOULD FURTHER INFORMATION BE GIVEN TO MIDMARK CORPORATION REGARDING THIS INSTANCE, A FOLLOW-UP REPORT WILL BE MADE.

    Description of Event or Problem · 0

    ON JULY 10, 2025, MIDMARK CORPORATION WAS NOTIFIED OF AN INSTANCE THAT OCCURRED ON OR AROUND ON (B)(6) 2025, IN WHICH CLEANING PERSONNEL WERE CLEANING A MODEL 224 EXAM TABLE. WHILE CLEANING THE TABLE, THE FOOT CONTROL WAS ACTIVATED AND THE TABLE DESCENDED ONTO THEIR FOOT. MIDMARK CORPORATION HAS MADE MULTIPLE ATTEMPTS FOR FURTHER INFORMATION OF THE CURRENT STATE OF THE TABLE AND ADDITIONAL DETAILS OF THIS INSTANCE, ALTHOUGH NO FURTHER DETAILS HAVE BEEN MADE AVAILABLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2664195 RITTER BARRIER FREE EXAM CHAIR GBB MIDMARK CORPORATION 224-002 00841709106002

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Other