BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    NA

    MDR report key: 24916552 · Received April 17, 2026

    Report

    Report Number
    8020021-2026-00007
    Event Type
    Malfunction
    Date Received
    April 17, 2026
    Report Date
    April 17, 2026
    Manufacturer
    GE HEALTHCARE AUSTRIA GMBH & CO OG
    Product Code
    ITX
    PMA / PMN Number
    K230346
    Removal / Correction Number
    Z-0865-2024
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FR
    Reporter Occupation
    003

    Narratives

    Additional Manufacturer Narrative · 0

    LEGAL MANUFACTURER: HCS KRETZ - TIEFENBACH 15 AUSTRIA ZIPF OBEROSTERREICH, 4871. GE HEALTHCARE REPORTED A FIELD MODIFICATION FOR THIS IC9-RS DOUBLE IMAGE MALFUNCTION PER 21 CFR 806 ON 29-DEC-2023. THE US-FDA RECALL NUMBER IS Z-0865-2024. CUSTOMERS WERE SENT A LETTER EXPLAINING THE ISSUE AND REQUESTING THE CUSTOMER TO PERFORM AN INSPECTION TEST TO DETERMINE IF THE PROBE IS MALFUNCTIONING. GE HEALTHCARE HAS DETERMINED THE CAUSE OF THE MALFUNCTIONING PROBE TO BE A PROBE COMPONENT.

    Description of Event or Problem · 0

    THE CUSTOMER REPORTED SEEING A DOUBLE IMAGE WITH THEIR IC9-RS DIAGNOSTIC ULTRASOUND PROBE TO GE HEALTHCARE. IT WAS CONCLUDED THE IC9-RS DIAGNOSTIC ULTRASOUND PROBE WAS IDENTIFIED AS HAVING A COMPONENT MALFUNCTION DESCRIBED IN US-FDA RECALL NO. Z-0865-2024 INITIATED BY GE HEALTHCARE ON (B)(6) 2023. THERE WAS NO IMPACT TO A PATIENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    593568 NA DIAGNOSTIC ULTRASOUND TRANSDUCER ITX GE HEALTHCARE AUSTRIA GMBH & CO OG IC9-RS

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown