BEUDAMED
    224 results · 17ms · Sources: EU EUDAMED, US FDA

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    Kit BD Max ExK DNA 1 USA; Catalog # 442817

    FDA Recall
    Terminated ·Becton Dickinson & Co.·Product code JJH·July 17, 2019

    Kit BD Max Enteric Bacterial Panel EU; Catalog # 442963

    FDA Recall
    Terminated ·Becton Dickinson & Co.·Product code PCH·July 17, 2019

    Kit BD Max MRSA; Catalog # 442953

    FDA Recall
    Terminated ·Becton Dickinson & Co.·Product code NQX·July 17, 2019

    Kit EXT Enteric Bacterial Panel; Catalog # 443812

    FDA Recall
    Terminated ·Becton Dickinson & Co.·Product code PCH·July 17, 2019

    Lev5, REF CT1587B, 50 Susceptibility discs Levofloxacin 5 ug, IVD, CE 2797

    FDA Recall
    Open, Classified ·Oxoid Limited Wade Road Basingstoke United Kingdom·Product code JTN·December 23, 2024

    Kit BD Max ExK DNA 2 EU LUO; Catalog # 442820

    FDA Recall
    Terminated ·Becton Dickinson & Co.·Product code N/A·July 17, 2019

    Kit BD Max ExK DNA 2 USA; Catalog # 442819

    FDA Recall
    Terminated ·Becton Dickinson & Co.·Product code JJH·July 17, 2019

    Kit BD Max Vaginal Panel; Catalog # 443712

    FDA Recall
    Terminated ·Becton Dickinson & Co.·Product code PQA·July 17, 2019

    Kit BD Max Check-Points CPO IVD EU; Catalog # 278102

    FDA Recall
    Terminated ·Becton Dickinson & Co.·Product code N/A·July 17, 2019

    BD VACUTAINER PLUS SST Tube with HEMOGARD closure 13x75mm 3.5ml PLBL Gold, Catalog No. 367983

    FDA Recall
    Terminated ·Becton Dickinson & Company·Product code JKA·February 13, 2018

    BD VACUTAINER PLUS SST Tube with HEMOGARD closure 13x100mm 5.0ml PLBL Gold, Catalog No. 367986

    FDA Recall
    Terminated ·Becton Dickinson & Company·Product code JKA·February 13, 2018

    Alaris EtCO2, Model 8300, UDI: 10885403830013, CareFusion for models 11634567 and 8300ADXeN933

    FDA Recall
    Terminated ·CareFusion 303, Inc.·Product code CCK·July 1, 2019

    BD Synapsys Microbiology Informatics Solution, Catalog Number 444150, Software Version 4.10

    FDA Recall
    Terminated ·Becton Dickinson & Co.·Product code JQP·March 9, 2022

    TSX-301A/2 Aquilion One CT System. The TSX-30IAl2 is a whole body CT scanner. This device captures cross sectional volume data sets. The device consists of a gantry, patient couch (table) and peripheral cabinets used for data processing and display. This device is intended to produce cross sectional volume sets of the anatomy. Additionally the system, when used by a trained professional, is capable of proving data for dynamic and perfusion studies of organs and extremities.

    FDA Recall
    Terminated ·Toshiba American Medical Systems Inc·Product code JAK·May 13, 2008

    BD Kiestra Urine Culture Application Powered by BD Synapsys Informatics Solution; Catalog (Ref): 444900;

    FDA Recall
    Open, Classified ·Becton Dickinson & Co.·Product code KZB·July 9, 2024

    BD Luer Tip Caps; Catalog Number(s) or Model Number(s): 308341;

    FDA Recall
    Open, Classified ·Becton Dickinson & Company·Product code KYW·October 14, 2025

    BD Alaris Syringe Module, REF 8110

    FDA Recall
    Open, Classified ·CareFusion 303, Inc.·Product code FRN·September 15, 2023

    Alaris PCA Module 8120

    FDA Recall
    Open, Classified ·CareFusion 303, Inc.·Product code FRN·September 15, 2023

    BD Anti-Kappa APC (Cat. No. 341098) is an analyte specific reagent for the Anti-Kappa antibody, which specifically recognizes the kappa light chains of human immunoglobulins. Anti-Kappa is used for in vitro identification of cells expressing the kappa light chains using flow cytometry.

    FDA Recall
    Open, Classified ·Becton, Dickinson and Company, BD Biosciences·Product code MVU·March 25, 2022

    BD Alaris PCU REF 8015

    FDA Recall
    Open, Classified ·CareFusion 303, Inc.·Product code FRN·September 15, 2023