1,757 results · 36ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

ATELLICA CH 930 ANALYZER

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JJE·June 23, 2020

UNKNOWN M/L TAPER STEM

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code KWA·February 3, 2017

UNKNOWN 32MM HEAD

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code KWY·January 31, 2017

UNKNOWN ML TAPER STEM

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code KWA·January 31, 2017

CARDIOSAVE HYBRID, 3.1 EDITION

FDA Adverse Event
Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·April 28, 2023

BD SEDI-40

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code GHC·June 12, 2018

TVT-S

FDA Adverse Event
Injury ·JNJ·Product code FTL·November 15, 2008

CARDIOSAVE HYBRID, TYPE B PLUG

FDA Adverse Event
Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·July 18, 2023

BD INSYTE AUTOGUARD

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code FOZ·April 26, 2024

UNSPECIFIED BD SYRINGE

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code FMF·September 15, 2022

EUFLEXXA INJ

FDA Adverse Event
Injury ·UNK·Product code MOZ·November 2, 2017

PEN INJ

FDA Adverse Event
Injury ·ELI LILLY AND COMPANY PHARMACEUTICAL DELIVERY SYSTEMS·Product code FMF·October 11, 2018

ORTHOVISC INJ

FDA Adverse Event
Injury ·ANIKA THERAPEUTICS INC.·Product code MOZ·April 30, 2019

MONOVISC INJ

FDA Adverse Event
Injury ·ANIKA THERAPEUTICS, INC.·Product code MOZ·January 24, 2020

UNSPECIFIED BD¿ PEN NEEDLE

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code FMI·August 8, 2023

UNSPECIFIED BD¿ PEN NEEDLE

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code FMI·October 12, 2023

UNSPECIFIED BD POSIFLUSH¿ SYRINGE

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code NGT·June 14, 2023

SZ 32 MM PINNACLE ALTRX POLYETHYLENE ACETABULAR

FDA Adverse Event
Injury ·JNJ DEPUY ORTHOPEDICS·Product code LPH·July 19, 2011

UNSPECIFIED BD PMCF-Q-SYTE-EXTENSION-SET

FDA Adverse Event
Injury ·BECTON DICKINSON·Product code FPA·April 14, 2021

CARDIOSAVE HYBRID, TYPE B PLUG

FDA Adverse Event
Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·July 3, 2024