BEUDAMED
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    FYI URINE PREGNANCY

    FDA UDI
    GERMAINE LABORATORIES, INC·00695684970383·Urine cassette test. For the rapid qualitative...

    PUBLIX WAXED FLOSS

    FDA Adverse Event
    Malfunction ·PUBLIX SUPER MARKETS, INC.·Product code JES·February 1, 2024

    BD INSYTE AUTOGUARD BC SHIELDED IV CATHETER

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL SYSTEMS·Product code FOZ·October 5, 2020

    ATRIAL LEAD

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, CARDIOLOGY DIVISION, INC.·Product code NVN·May 28, 2024

    INFUSOMAT SPACE - US VERSION

    FDA Adverse Event
    Malfunction ·B. BRAUN MELSUNGEN AG·Product code FRN·April 17, 2014

    STOCKERT SIII

    FDA Adverse Event
    Malfunction ·COBE CARDIOVASCULAR, INC.·Product code DTQ·November 17, 2008

    IMPLANTABLE CARDIOVERTER DEFIBRILLATOR (NON-CRT)

    FDA Adverse Event
    Malfunction ·MEDTRONIC·Product code LWS·August 11, 2023

    LIFESCAN SURESTEP PRO GLUCOMETER STRIPS

    FDA Adverse Event
    Malfunction ·LIFESCAN·Product code CGA·March 19, 2010

    RONGUER, IVD CUSHING

    FDA Adverse Event
    Malfunction ·BD/ V. MUELLER·Product code HAE·January 6, 2017

    MEDLINE INDUSTRIES, INC.

    FDA Adverse Event
    Malfunction ·MEDLINE INDUSTRIES, INC.·Product code FSM·November 25, 2024

    PERI-LOC

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC., ORTHOPAEDIC DIV.·Product code HRS·May 28, 2008

    BARD FOLEY CATHETER

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC.·Product code KOD·September 23, 1998

    BD ALARIS¿ SMARTSITE¿ LOW SORBING SECONDARY SET

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS, S.A. DE C.V.·Product code FPA·January 12, 2023

    LEAD

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code NVY·August 12, 2023

    PERMANENT DEFIBRILLATOR ELECTRODES

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code NVY·August 12, 2023

    EZ IO 45MM NEEDLE SET + STABILIZER

    FDA Adverse Event
    Injury ·TELEFLEX MEDICAL·Product code FMI·September 19, 2025

    MEDTRONIC LEAD

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code DXY·August 12, 2023

    VALVE AORTIC 21MM

    FDA Adverse Event
    Injury ·SORIN GROUP ITALIA S.R.L. / LIVANOVA USA, INC.·Product code PMA·July 15, 2019

    ACS HI-TORQUE FLOPPY II

    FDA Adverse Event
    Malfunction ·GUIDANT CORP. ADVANCED CARDIOVASCULAR SYSTEMS·Product code DQX·April 28, 1998

    MALEM BEDWETTING ALARM

    FDA Adverse Event
    Injury ·MALEM MEDICAL·Product code KPN·November 28, 2017