BEUDAMED
    7 results · 12ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Recall × Status: Open, Classified × Clear all

    LUMINOS Lotus Max, Model 11574100 and Luminos dRF Max, Model 10762471

    FDA Recall
    Open, Classified ·Siemens Medical Solutions USA, Inc·Product code OWB·December 5, 2025

    FGFR RGQ RT-PCR Kit (RUO, not IVD) REF 8747010

    FDA Recall
    Open, Classified ·Qiagen Sciences LLC·Product code OWD·July 20, 2022

    therascreen FGFR RGQ RT-PCR kit (US IVD) REF 874721

    FDA Recall
    Open, Classified ·Qiagen Sciences LLC·Product code OWD·July 20, 2022

    therascreen KRAS RGQ PCR Kit (24) Model Number(s): REF 870021 (US IVD)

    FDA Recall
    Open, Classified ·Qiagen Sciences LLC·Product code OWD·February 25, 2022

    therascreen KRAS RGQ PCR Kit (24) REF 874052 (Japan IVD, not released in the USA)

    FDA Recall
    Open, Classified ·Qiagen Sciences LLC·Product code OWD·February 25, 2022

    therascreen FGFR RGQ RT-PCR Kit (CE IVD, not sold in the US) REF 874711

    FDA Recall
    Open, Classified ·Qiagen Sciences LLC·Product code OWD·July 20, 2022

    therascreen KRAS RGQ PCR Kit (24)-IVD qualitative PCR assay used on the Rotor-Gene Q MDx instrument for the detection of seven somatic mutations in the human KRAS oncogene REF 870021 (US IVD)

    FDA Recall
    Open, Classified ·Qiagen GmbH Qiagen Str. 1 Hilden Germany·Product code OWD·August 22, 2023