BEUDAMED
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    BD PHASEAL

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code ONB·May 8, 2026

    HUMALOG 75/25 KWIKPEN

    FDA Adverse Event
    Malfunction ·ELI LILLY·Product code FMF·October 7, 2016

    MONOJCT 20ML SYR L-LOCK

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH·Product code FMF·June 23, 2022

    STIM Q

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code GZF·August 9, 2023

    MONOJCT 60ML SYR L-LOCK BNS

    FDA Adverse Event
    Malfunction ·CARDINAL HEALTH·Product code FMF·December 6, 2021

    35ML SYRINGE LUER LOCK TIP RP

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FMF·June 30, 2021

    UNKNOWN NEEDLES AND SYRINGES

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FMF·May 1, 2020

    1915484-2017-05031

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code LZH·June 1, 2017

    VICRYL PLUS SUTURE 27"(70CM) 3-0 VIO

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAM·November 26, 2024

    IMPLANTED PICC

    FDA Adverse Event
    Injury ·BARD REYNOSA S.A. DE C.V.·Product code LJS·June 8, 2012

    ON-Q PAINBUSTER

    FDA Adverse Event
    Other ·I-FLOW CORP.·Product code MEB·August 31, 2010

    LEAD

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code NVY·December 3, 2025

    GEM V/NV 20D 1CV 2SS DEHP FREE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FPA·May 13, 2024

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·April 20, 2023

    BD PHASEAL OPTIMA

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code ONB·May 14, 2026

    ON-Q C-BLOC WITH SELECT-A-FLOW

    FDA Adverse Event
    Other ·I-FLOW CORP.·Product code MEB·May 12, 2009

    ON-Q C BLOC

    FDA Adverse Event
    Injury ·KIMBERLY CLARK / IFLOW·Product code MEB·April 21, 2014

    1ML BBL SHORT REG WOS UPT 3622

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code FMF·August 11, 2020

    RIGHT VENTRICULAR LEAD

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, CARDIOLOGY DIVISION, INC.·Product code NVY·May 22, 2024

    THUNDERBEAT 5 MM, 35 CM, FRONT-ACTUATED GRIP

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code GEI·October 28, 2021