BEUDAMED
    FDA Recall Open, Classified

    BD Pyxis Mini Main REF: 349 Medication cabinet

    Recall: Z-2301-2026 · Initiated April 30, 2026

    Recall

    Recall Number
    Z-2301-2026
    Event Number
    98895
    Firm
    CareFusion 303, Inc.
    FEI Number
    2016493
    Product Code
    BRY
    Status
    Open, Classified
    Root Cause
    Component design/selection
    Initiated
    April 30, 2026
    Posted
    June 3, 2026
    Address
    10020 Pacific Mesa Blvd, San Diego, CA, 92121-4386

    Description

    BD Pyxis Mini Main REF: 349 Medication cabinet

    Reason

    Fingerprint scanner may overheat to a temperature to cause 1st degree burn.

    Action

    On April 30, 2026, CareFusion (subsidiary of Becton, Dickinson and Company) issued a Urgent Medical Device Recall Notification, via mail or Email. CareFusion ask consignees to take the following actions: 1. Dispensing cabinets can continue to be used as intended. 2. If you suspect that the Bio-ID Scanner is hot, please discontinue the use of Scanner and file a complaint. 3. Review and update facility policies and procedures related to situations where the Bio-ID Scanner is unavailable to mitigate delays in care. 4. Complete the attached Customer Response Form and return to the BD contact noted on the form.

    Distribution

    US: Nationwide OUS: AE, AU, BE, BH, BR, CA, CL, ES, GB, IT, KW, MA, MX, NZ, PT, QA, SA, SG, TH, TW

    Quantity

    709 units