BEUDAMED
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    Atellica Gamma-Glutamyl Transferase (GGT) Reagent - Product Usage: For in vitro diagnostic use in the quantitative determination of gamma-glutamyl transferase in human serum and plasma. Siemens Material Number (SMN): 11097597

    FDA Recall
    Open, Classified ·Siemens Healthcare Diagnostics, Inc.·Product code JQA·November 23, 2020

    Atellica CH Gamma-Glutamyl Transferase-IIn vitro diagnostic use in the quantitative determination of gamma-glutamyl transferase in human serum and plasma (lithium heparin Test Code: GGT Siemens Material Number (SMN): 11097597

    FDA Recall
    Open, Classified ·Siemens Healthcare Diagnostics, Inc.·Product code JFM·July 10, 2023

    ADVIA Gamma-Glutamyl Transferase (GGT) Reagent - Product Usage: For in vitro diagnostic use in the quantitative determination of gamma-glutamyl transferase in human serum and plasma. Siemens Material Number (SMN): ADVIA Chemistry: 10309495 (20 mL) 10316298 (70 mL)

    FDA Recall
    Open, Classified ·Siemens Healthcare Diagnostics, Inc.·Product code JQA·November 23, 2020

    Atellica CH HDL Cholesterol- In vitro diagnostic use in the quantitative determination of HDL cholesterol in human serum and plasma (lithium heparin, EDTA, sodium Heparin) Test Code: HDLC Siemens Material Number (SMN): 11537213

    FDA Recall
    Open, Classified ·Siemens Healthcare Diagnostics, Inc.·Product code JFM·July 10, 2023

    Atellica CH LDL Cholesterol- In vitro diagnostic use in the quantitative determination of LDL cholesterol in human serum and plasma (lithium heparin, EDTA, sodium heparin Test Code: LDLC Siemens Material Number (SMN): 11537214

    FDA Recall
    Open, Classified ·Siemens Healthcare Diagnostics, Inc.·Product code JFM·July 10, 2023

    Atellica CH Total Bilirubin_2 -In vitro diagnostic use in the quantitative determination of total bilirubin in human serum and plasma (lithium heparin) of adults and neonates Test Code: TBil_2 Siemens Material Number (SMN): 11097531

    FDA Recall
    Open, Classified ·Siemens Healthcare Diagnostics, Inc.·Product code JFM·July 10, 2023

    Atellica IM Erythropoietin (EPO) Assay (100 Test)

    FDA Recall
    Open, Classified ·Siemens Healthcare Diagnostics, Inc.·Product code GGT·January 24, 2024

    ADVIA Centaur Erythropoietin (EPO) Assay (100 Test)

    FDA Recall
    Open, Classified ·Siemens Healthcare Diagnostics, Inc.·Product code GGT·January 24, 2024

    Quantikine IVD Erythropoietin Human Serum Controls for use as quantitative controls for the determination of Erythropoietin concentrations in human serum and plasma. IFU, Part Number 750095

    FDA Recall
    Open, Classified ·R & D Systems, Inc.·Product code GGT·June 14, 2022

    Access Erythropoietin (EPO), Catalog Number - A16364 a glycoprotein (~30,400 Daltons) produced primarily by the kidney, is the principal factor regulating red blood cell production (erythropoiesis) in mammals. Renal production of EPO is regulated by changes in oxygen availability. Under conditions of hypoxia, the level of EPO in the circulation increases and this leads to increased production of red blood cells.

    FDA Recall
    Open, Classified ·Beckman Coulter, Inc.·Product code GGT·February 3, 2025

    Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181030

    FDA Recall
    Open, Classified ·TELEFLEX LLC·Product code BTR·May 25, 2023

    Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181055

    FDA Recall
    Open, Classified ·TELEFLEX LLC·Product code BTR·May 25, 2023

    Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180060

    FDA Recall
    Open, Classified ·TELEFLEX LLC·Product code BTR·May 25, 2023

    Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180050

    FDA Recall
    Open, Classified ·TELEFLEX LLC·Product code BTR·May 25, 2023

    Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180065

    FDA Recall
    Open, Classified ·TELEFLEX LLC·Product code BTR·May 25, 2023

    Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181040

    FDA Recall
    Open, Classified ·TELEFLEX LLC·Product code BTR·May 25, 2023

    Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180070

    FDA Recall
    Open, Classified ·TELEFLEX LLC·Product code BTR·May 25, 2023

    Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181065

    FDA Recall
    Open, Classified ·TELEFLEX LLC·Product code BTR·May 25, 2023

    Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100180040

    FDA Recall
    Open, Classified ·TELEFLEX LLC·Product code BTR·May 25, 2023

    Preformed AGT Oral Endotracheal Tube uncuffed/plain - Murphy, REF 100181050

    FDA Recall
    Open, Classified ·TELEFLEX LLC·Product code BTR·May 25, 2023