BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ADVANCED TABLE, OPERATING-ROOM, ELECTRICAL

    MDR report key: 25178632 · Received May 14, 2026

    Report

    Report Number
    3006697241-2026-00183
    Event Type
    Injury
    Date Received
    May 14, 2026
    Date of Event
    April 20, 2026
    Report Date
    May 14, 2026
    Manufacturer
    BAXTER HEALTHCARE CORPORATION
    Product Code
    GDC
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 0

    NO FURTHER INFORMATION IS AVAILABLE ON THE REPAIR OF THE BED/DEVICE AT THIS TIME. THE INVESTIGATION IS ONGOING, HOWEVER IF ANY ADDITIONAL RELEVANT INFORMATION IS IDENTIFIED FOLLOWING THE COMPLETION OF THE INVESTIGATION, THE ADDITIONAL RELEVANT INFORMATION WILL BE SUBMITTED IN A SUPPLEMENTAL REPORT.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT A FACILITY STAFF MEMBER INJURED HIS FINGER WHILE TRANSPORTING THE ALLEN ADVANCE SURGICAL TABLE. THE STAFF MEMBER WAS ATTEMPTING TO TRANSPORT THE TABLE AT THE TIME OF THE EVENT, AND HIS FINGER WAS INADVERTENTLY CAUGHT AND PINCHED BY A COMPONENT OF THE TABLE¿S FOOT END COLUMN. THE FORCE RESULTED IN A TUFT FRACTURE, AS WELL AS A LACERATION TO THE FINGER WHICH REQUIRED SUTURE REPAIR. NO MEDICAL INTERVENTION WAS REPORTED FOR THE ALLEGED FRACTURE. THE DEVICE INSTRUCTIONS FOR USE IDENTIFIES AND CAUTIONS THE USER OF PINCH POINTS ON THE TABLE AND THAT THE TABLE SHOULD BE OPERATED BY TRAINED PERSONS ONLY. THE INSTRUCTIONS FOR USE WARNING THE USER TO BE AWARE OF THIS PINCH POINT ON THE TABLE DURING TRANSPORT " BETWEEN AN H-BRACKET AND THE COLUMN". THE CAUSE OF THE EVENT IS ATTRIBUTED TO THE ACCIDENTAL PLACEMENT OF THE STAFF MEMBER¿S HAND/FINGERS COMBINED WITH THE UNINTENTIONAL MOVEMENT OF THE TABLE COLUMN COMPONENT THAT OCCURRED DURING TRANSPORT OF THE DEVICE. THERE WAS NO REPORT OF A DEVICE MALFUNCTION. NO FURTHER INFORMATION WAS AVAILABLE AT THE TIME OF THIS REPORT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    49267 ADVANCED TABLE, OPERATING-ROOM, ELECTRICAL TABLE, OPERATING-ROOM, ELECTRICAL GDC BAXTER HEALTHCARE CORPORATION A-71100-A2

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Required Intervention N/A.