109 results · 82ms · Sources: EU EUDAMED, US FDA

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KENDRICK

FDA Adverse Event
Malfunction ·EMERGENCY PRODUCTS AND RESEARCH·Product code IQF·July 2, 2008

INFINION 16

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·May 11, 2023

ZENITION

FDA Adverse Event
Malfunction ·PHILIPS INDIA LTD.·Product code OWB·July 19, 2024

SPEAKMAN EYMEDIC SE-4270 SINGLE USE CONTAINER WATER, USP

FDA Adverse Event
Malfunction ·SPEAKMAN·Product code LWD·March 28, 2005

TORQUE SHAFT

FDA Adverse Event
Malfunction ·DEPUY SYNTHES SPINE·Product code LXH·December 26, 2012

BD PLASTIPAK¿ SYRINGE LUER SLIP

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·November 27, 2017

AMPLATZER AMULET

FDA Adverse Event
Malfunction ·ABBOTT MEDICAL·Product code NGV·November 24, 2025

BD PAXGENE® BLOOD DNA

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code PJE·March 26, 2019

UNKNOWN DISPOSABLE SET

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code FPA·April 28, 2024

SCREWDRIVER, SYSTEM UNKNOWN

FDA Adverse Event
Malfunction ·DEPUY RAYNHAM·Product code LXH·August 27, 2012

PORTICO TRANSCATHETER AORTIC VALVE

FDA Adverse Event
Malfunction ·ABBOTT MEDICAL·Product code NPT·October 2, 2025

10 ML BD POSIFLUSH¿ NORMAL SALINE SYRINGE

FDA Adverse Event
Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·March 31, 2020

HEARTMATE 3 LEFT VENTRICULAR ASSIST SYSTEM

FDA Adverse Event
Malfunction ·THORATEC CORPORATION·Product code DSQ·November 26, 2020

BD SYRINGE

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·June 24, 2020

THORATEC® HEARTMATE 3® LVAS IMPLANT KIT

FDA Adverse Event
Malfunction ·THORATEC CORPORATION·Product code DSQ·November 15, 2024

THORATEC® HEARTMATE 3® LVAS IMPLANT KIT

FDA Adverse Event
Malfunction ·THORATEC CORPORATION·Product code DSQ·January 14, 2025

L&ERESEARCH-NEXIVA-2024

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·May 1, 2024

BD VACUTAINER K2E 3.6MG PLUS BLOOD COLLECTION TUBES

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·July 6, 2021

CONFIDENCE INTRO NEEDLE, DIA, 10G 5

FDA Adverse Event
Malfunction ·DEPUY RAYNHAM·Product code GAA·December 18, 2012

3M

FDA Adverse Event
Malfunction ·3M COMPANY·Product code FXX·February 17, 2021