BEUDAMED
    FDA Adverse Event Other Summary report: N

    AIRLIFE 2025 EDITION BROSELOW TAPE 36-2446 REV. 3

    MDR report key: 23582569 · Received November 18, 2025

    Report

    Report Number
    MW5178966
    Event Type
    Other
    Date Received
    November 18, 2025
    Date of Event
    November 12, 2025
    Report Date
    November 13, 2025
    Manufacturer
    SUNMED GROUP HOLDINGS, LLC DBA AIRLIFE
    Product Code
    OKI
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    PHARMACIST
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    VIA THE MEDICATION SAFETY SOCIETY ORGANIZATION WEBSITE, WE WERE ALERTED TO NEW ERRORS ON THE BROSELOW TAPE 36-23446 REV. 3. UNDER THE CALCULATIONS BASIS SECTION. FOR ERROR #1- PLEASE SEE AIRWAY MANAGEMENT SECTION - PRE-RSI/RSA NEUROMUSCULAR BLOCKERS. THE VECURONIUM UNITS ARE LISTED AS MG/ML-SHOULD BE MG/KG. FOR ERROR #2, PLEASE SEE THE TOXICOLOGY SECTION (800-222-1222). THE FLUMAZENIL DOSE LISTED AS 0.1 MG/KG- SHOULD BE 0.01 MG/KG. I SPOKE THE AIRLIFE REPRESENTATIVE AND I WAS INFORMED THEY WERE MADE AWARE OF THE ERROR ON 10/30/25. I CANNOT FIND ANY NOTIFICATION INFORMING HOSPITALS OR OTHER USERS OF THE ERROR. REVISION 2 OF THE BROSELOW TAPE WAS RECALLED DUE TO ERRORS NOW REVISION 3 ALSO HAS ERRORS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2362784 AIRLIFE 2025 EDITION BROSELOW TAPE 36-2446 REV. 3 EMERGENCY RESPONSE SAFETY KIT OKI SUNMED GROUP HOLDINGS, LLC DBA AIRLIFE 36-234446

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Other