BEUDAMED
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    VACUTAINER

    FDA Adverse Event
    Injury ·BECTON DICKINSON VACUTAINER SYSTEMS·Product code GIO·October 8, 1992

    VACUTAINER REDUCED DRAW CITRATE TUBE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON VACUTAINER SYSTEMS·Product code JKA·December 6, 1996

    BECTON DICKINSON VACUTAINER SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code JKA·November 21, 2000

    BECTON DICKINSON VACUTAINER SYSTEMS

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO.·Product code JKA·January 24, 2000

    Microtainer Safety Flow Lancets; Green Sterile, Use Once and Discard; 1.4 mm Blade Length; 1.0mm Blade Width; Becton Dickinson Vacutainer Systems; Becton Dickinson & Company; Franklin Lakes, NJ 07417

    FDA Recall
    Terminated ·Becton Dickinson & Company·Product code FMK·September 26, 2007

    Microtainer Safety Flow Lancets; Blue Sterile Use once and Discard; 1.9mm Blade Length; 1.0 mm Blade Width; Becton Dickinson Vacutainer Systems Becton dickinson and COmpany; Franklin Lakes, NJ 07417

    FDA Recall
    Terminated ·Becton Dickinson & Company·Product code F·September 26, 2007

    Microtainer Safety flow Lancets; Yellow Sterile Use once and discard; 2.2mm Blade Length; 1.0mm blade width; Becton Dickinson Vacutainer System; Becton Dickinson and Company; Franklin Lakes, NJ 07417

    FDA Recall
    Terminated ·Becton Dickinson & Company·Product code F·September 26, 2007

    ARCHITECT C8000 SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING, INC.·Product code JJE·March 23, 2009

    ARCHITECT C8000 SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING, INC.·Product code MZV·March 23, 2009

    BD VACUTAINER PUSH BUTTON BLOOD COLLECTION SET

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code JKA·May 5, 2021

    BD VACUTAINER PUSH BUTTON BLOOD COLLECTION SET

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code JKA·December 2, 2020

    BD VACUTAINER BLOOD ALCOHOL DETERMINATIONS SODIUM FLUORIDE POTASSIUM OXALATE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·April 8, 2021

    BD VACUTAINER PUSH BUTTON BLOOD COLLECTION SET

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code JKA·November 19, 2020

    BD VACUTAINER PUSH BUTTON BLOOD COLLECTION SET

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code JKA·November 3, 2020

    SYSMEX CA-660 ANALYZER

    FDA Adverse Event
    Other ·SYSMEX CORPORATION·Product code GKP·June 16, 2014

    BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code JKA·February 9, 2022

    Magellan Diagnostics LeadCare Ultra Blood Analyzer Part Number: 80-0010

    FDA Enforcement
    Class I ·Terminated·Magellan Diagnostics, Inc.·May 24, 2017

    Magellan Diagnostics LeadCare Ultra Blood Lead Test Kits Part Number: 80-0010

    FDA Enforcement
    Class I ·Terminated·Magellan Diagnostics, Inc.·May 24, 2017

    UNICEL® DXI 800 ACCESS® IMMUNOASSAY SYSTEM

    FDA Adverse Event
    Injury ·BECKMAN COULTER, INC.·Product code DHA·December 10, 2012

    ARCHITECT C8000 SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING, INC.·Product code JJE·December 3, 2008