BEUDAMED
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    Filters Regulation: Us FDA × Status: Malfunction × Clear all

    BARD POWERMIDLINE CATHETER (4F) (SINGLE-LUMEN) (20CM)

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (BASD) -3006260740·Product code PND·May 13, 2022

    PRO-LINE CT

    FDA Adverse Event
    Malfunction ·MEDICAL COMPONENTS, INC.·Product code LJS·August 23, 2024

    ALARIS

    FDA Adverse Event
    Malfunction ·ALARIS MEDICAL SYSTEMS INC·Product code FPA·March 7, 2005

    POWERED 60 ECHELON +, 440MM SHAFT

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·September 27, 2021

    ILET BIONIC PANCREAS

    FDA Adverse Event
    Malfunction ·BETA BIONICS INC.·Product code QFG·December 11, 2025

    MITYVAC

    FDA Adverse Event
    Malfunction ·PRISM HEALTH CARE·Product code HDB·November 28, 2003

    TRUEMETRIX

    FDA Adverse Event
    Malfunction ·TRIVIDIA HEALTH, INC.·Product code NBW·September 19, 2019

    MINI ONE® BALLOON BUTTON

    FDA Adverse Event
    Malfunction ·APPLIED MEDICAL TECHNOLOGY, INC.·Product code KNT·July 15, 2025

    FLEXIFLO PATROL ENTERAL PUMP

    FDA Adverse Event
    Malfunction ·ROSS PRODUCTS DIVISION, ABBOTT LABORATORIES·Product code LZH·December 1, 2003

    PPROXIMATE ILS INTARLUMINAL STAPLER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GAG·December 23, 1996

    EXCOR

    FDA Adverse Event
    Malfunction ·BERLIN HEART GMBH·Product code DSQ·October 29, 2025

    ENDOPATH ARTICULATING LINEAR STAPLER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GAG·December 23, 1996

    CLEARLINK/CONTINU-FLO

    FDA Adverse Event
    Malfunction ·BAXTER INTERNATIONAL INC.·Product code FPA·May 17, 2024

    EXACTAMIX

    FDA Adverse Event
    Malfunction ·BAXTER CORPORATION ENGLEWOOD·Product code NEP·September 8, 2021

    BARD POWERMIDLINE CATHETER (4F) (SINGLE-LUMEN) (20CM)

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (BASD) -3006260740·Product code PND·May 13, 2022

    BARD POWERMIDLINE CATHETER (4F) (SINGLE-LUMEN) (20CM)

    FDA Adverse Event
    Malfunction ·C.R. BARD, INC. (BASD) -3006260740·Product code PND·May 12, 2022

    FIRST PICC¿ S/L PERIPHERALLY INSERTED CENTRAL CATHETER

    FDA Adverse Event
    Malfunction ·ARGON MEDICAL DEVICES·Product code FOZ·April 19, 2023

    L-CATH PICC D/L 20GA (2.6F) 0.90MM X 60CM

    FDA Adverse Event
    Malfunction ·ARGON MEDICAL DEVICES·Product code LJS·May 10, 2023

    ACCU-CHEK ® COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·July 25, 2011

    PEG NEEDLE

    FDA Adverse Event
    Malfunction ·BARD·Product code KNT·February 5, 2014