BEUDAMED
    FDA Adverse Event Injury Summary report: N

    RITTER

    MDR report key: 22635093 · Received July 28, 2025

    Report

    Report Number
    1523530-2025-00005
    Event Type
    Injury
    Date Received
    July 28, 2025
    Date of Event
    July 2, 2025
    Report Date
    July 28, 2025
    Manufacturer
    MIDMARK CORPORATION
    Product Code
    GBB
    UDI-DI
    00841709106002
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OR, US
    Reporter Occupation
    NURSE
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    ON JULY 2, 2025, MIDMARK CORPORATION WAS NOTIFIED OF AN INSTANCE THAT OCCURRED ON OR AROUND (B)(6) 2025, IN WHICH A NURSE WAS PREPARING A PROCEDURE BED FOR A PATIENT. WHILE DOING SO, THE MODEL 224 EXAM TABLE FOOT CONTROL WAS ACTIVATED AND THE TABLE DESCENDED ONTO THE NURSE'S FOOT CAUSING AN ALLEGED BREAK TO THE RIGHT GREAT TOE. MIDMARK CORPORATION HAS MADE MULTIPLE ATTEMPTS FOR FURTHER INFORMATION OF THIS INSTANCE WITH NO FURTHER DETAILS 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 2, 2025, MIDMARK CORPORATION WAS NOTIFIED OF AN INSTANCE THAT OCCURRED ON OR AROUND (B)(6) 2025, IN WHICH A NURSE WAS PREPARING A PROCEDURE BED FOR A PATIENT. WHILE DOING SO, THE MODEL 224 EXAM TABLE FOOT CONTROL WAS ACTIVATED AND THE TABLE DESCENDED ONTO THE NURSE'S FOOT CAUSING AN ALLEGED BREAK TO THE RIGHT GREAT TOE. MIDMARK CORPORATION HAS MADE MULTIPLE ATTEMPTS FOR FURTHER INFORMATION OF THIS INSTANCE WITH NO FURTHER DETAILS MADE AVAILABLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1773875 RITTER BARRIER FREE EXAM CHAIR GBB MIDMARK CORPORATION 224-002 00841709106002

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Other