BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EDISON

    MDR report key: 24702591 · Received March 26, 2026

    Report

    Report Number
    3027664504-2026-00008
    Event Type
    Injury
    Date Received
    March 26, 2026
    Date of Event
    February 13, 2026
    Report Date
    March 25, 2026
    Manufacturer
    HISTOSONICS, INC.
    Product Code
    QGM
    UDI-DI
    00850006962082
    PMA / PMN Number
    K241902
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    PHYSICIAN
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    NO DEVICE MALFUNCTIONS OR OTHER NOTEWORTHY EVENTS OCCURRED DURING THE CASE. IN RESPONSE TO REPORTS OF ACUTE KIDNEY INJURY ASSOCIATED WITH HISTOTRIPSY, HISTOSONICS HAS INCORPORATED THE FOLLOWING WARNING INTO ITS LABELING: "CONSIDER PATIENT-SPECIFIC RISK FACTORS FOR ACUTE KIDNEY INJURY (AKI) AND/OR RENAL FAILURE BASED ON CLINICAL HISTORY AND PROCEDURAL SCENARIOS THAT COULD INCREASE STRESS ON KIDNEY FUNCTION, INCLUDING BUT NOT LIMITED TO HYDRATION STATUS, PLANNED TREATMENT VOLUME AND EXPECTED USE OF IMAGING CONTRAST AGENTS. CONSISTENT WITH OTHER LIVER-DIRECTED THERAPIES, TREATMENTS INVOLVING LARGE TREATMENT VOLUMES OR MULTIPLE TREATMENT SESSIONS MAY BE ASSOCIATED WITH AN INCREASED RISK OF AKI. EVALUATE RENAL RISK AND MONITOR FOR SIGNS OF AKI BEFORE AND AFTER TREATMENT."

    Description of Event or Problem · 0

    ON (B)(6) 2026, A 61-YEAR-OLD MALE WITH A HISTORY OF STAGE IV LEFT-SIDED COLON CANCER WITH METACHRONOUS LIVER METASTASES RECEIVED HISTOTRIPSY TREATMENT TO A SINGLE TUMOR IN LIVER SEGMENT 5 FOR A TOTAL PLANNED TREATMENT VOLUME (PTV) OF 17.3 CC. ON (B)(6), THE PATIENT PRESENTED TO THE EMERGENCY DEPARTMENT AND WAS SUBSEQUENTLY ADMITTED FOR EVALUATION OF ELEVATED SERUM CREATININE GREATER THAN 3.5 MG/DL AND SUSPECTED ACUTE KIDNEY INJURY (AKI). THE PATIENT RECEIVED INTRAVENOUS HYDRATION AND RENAL FUNCTION IMPROVED. THE CONDITION RESOLVED WITHOUT ADDITIONAL INTERVENTIONS, AND THE PATIENT WAS DISCHARGED ON (B)(6).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    765109 EDISON Focused ultrasound system for non-thermal, mechanical tissue ablation QGM HISTOSONICS, INC. 00850006962082

    Patients

    Seq Age Sex Outcome Treatment
    1 61 YR Male Hospitalization| O