BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRITON CANISTER

    MDR report key: 16632338 · Received March 28, 2023

    Report

    Report Number
    3011157718-2023-00019
    Event Type
    Malfunction
    Date Received
    March 28, 2023
    Date of Event
    November 8, 2019
    Report Date
    March 28, 2023
    Manufacturer
    STRYKER INSTRUMENTS-A DIVISION OF STRYKER CORP
    Product Code
    PBZ
    PMA / PMN Number
    K142801
    Removal / Correction Number
    Z-1186-2023
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 0

    PER THE CUSTOMER, THERE IS A CONCERN IN REGARDS TO PERCEIVED LOW EBL ON A CASE. TWO CANISTERS WERE SCANNED WITH A TOTAL EBL BETWEEN THE TWO OF 204. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITHOUT A SURGICAL DELAY. NO MEDICAL INTERVENTION OR ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    413 TRITON CANISTER IMAGE PROCESSING DEVICE FOR ESTIMATION OF EXTERNAL BLOOD LOSS PBZ STRYKER INSTRUMENTS-A DIVISION OF STRYKER CORP

    Patients

    Seq Age Sex Outcome Treatment
    1 Unknown