BEUDAMED
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    Filters FDA Adverse Event ×

    BD AUTOSHIELD¿ DUO PEN NEEDLE

    FDA Adverse Event
    Injury ·BECTON DICKINSON AND CO.·Product code FMI·January 4, 2019

    HEALICOIL RSB SA 5.5MM W/1 UT & 1 UB BLK

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MAI·March 3, 2021

    CADD LEGACY PCA PUMPS

    FDA Adverse Event
    Malfunction ·ICU MEDICAL, INC.·Product code MEA·August 6, 2025

    DREAMSTATION AUT

    FDA Adverse Event
    Injury ·RESPIRONICS, INC.·Product code BZD·April 7, 2022

    BIPAP AUT

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·July 6, 2022

    AUT SUTURE

    FDA Adverse Event
    Malfunction ·UNITED STATES SURGICAL·Product code GCJ·February 3, 2009

    DREAMSTATION AUT

    FDA Adverse Event
    Injury ·RESPIRONICS, INC.·Product code BZD·March 29, 2022

    FRESENIUS CATS AUT

    FDA Adverse Event
    Malfunction ·FRESENIUS KABI, LLC.·Product code CAC·October 4, 2016

    ACRA-CUT

    FDA Adverse Event
    Malfunction ·ACRA CUT·Product code HBF·November 30, 2001

    ACRA CUT

    FDA Adverse Event
    Injury ·ACRA CUT·Product code HBE·September 6, 2012

    DISPOSABLE SKULL PERFORATOR

    FDA Adverse Event
    Malfunction ·ACRA CUT·Product code KAT·July 31, 1992

    DISPOSABLE CRANIAL PERFORATOR

    FDA Adverse Event
    Malfunction ·ACRA CUT·Product code HBF·January 26, 1996

    ACRA CUT DISPOSABLE CRANIAL PERFORATOR 14MM DGRI

    FDA Adverse Event
    Malfunction ·ACRA-CUT·Product code HBF·August 26, 2010

    BILIARY STENT

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FGE·December 9, 2019

    ZIMMON BILIARY STENT

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·May 5, 2021

    TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code NIQ·August 3, 2004

    ACRA-CUT

    FDA Adverse Event
    Malfunction ·ACRA-CUT INC.·Product code HBF·June 30, 2010

    DISPOSABLE CRANIAL PERFORATOR

    FDA Adverse Event
    Malfunction ·ACRA-CUT, INC.·Product code HBF·June 29, 2012

    CRANIAL PERFORATORS

    FDA Adverse Event
    Malfunction ·ACRA-CUT, INC.·Product code HBF·November 17, 2003

    ACRA

    FDA Adverse Event
    Malfunction ·ACRA-CUT, INC·Product code HBF·September 22, 2000