515 results · 48ms · Sources: EU EUDAMED, US FDA

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PROSTHESIS, RIB REPLACMENT

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code MDI·April 24, 2014

BD VACUTAINER® K2E (EDTA) 18.0MG PLUS BLOOD COLLECTION TUBE

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·November 6, 2022

WHOLE GENOME SEQUENCING, SEQUENCING.COM

FDA Adverse Event
Malfunction ·UNK·Product code PFF·September 30, 2025

EVOLIS

FDA Adverse Event
Other ·STRATEC BIOMEDICAL SYSTEMS AG,·Product code JQW·May 25, 2007

EVIS LUCERA ELITE BRONCHOVIDEOSCOPE

FDA Adverse Event
Injury ·AIZU OLYMPUS CO., LTD.·Product code EOQ·October 5, 2023

BD VACUTAINER® PST¿ TUBES

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code JKA·May 9, 2018

ULTRASONIC PROBE

FDA Adverse Event
Injury ·SHIRAKAWA OLYMPUS CO., LTD.·Product code ITX·October 5, 2023

HEARTMATE 3 LVAS IMPLANT KIT

FDA Adverse Event
Death ·THORATEC CORPORATION·Product code DSQ·May 8, 2025

GENETIC SYSTEMS HIV-1/HIV-2 PLUS O EIA

FDA Adverse Event
Other ·BIO-RAD LABORATORIES, INC.·Product code MZF·November 19, 2007

AMPLATZER AMULET DELIVERY SYSTEM

FDA Adverse Event
Injury ·ABBOTT MEDICAL·Product code MLV·February 26, 2021

SYNCHROMED II

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·September 6, 2019

DEEP TRANSCRANIAL MAGNETIC STIMULATOR

FDA Adverse Event
Injury ·BRAINSWAY LTD.·Product code OBP·April 19, 2026

SYRINGE, PISTON

FDA Adverse Event
Malfunction ·BD / BECTON DICKINSON·Product code FMF·July 16, 2025

NATERA NIPT

FDA Adverse Event
Malfunction ·NATERA·Product code MAO·April 21, 2022

INDURA

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·December 12, 2015

PLATE

FDA Adverse Event
Death ·UNK·Product code HRS·February 29, 2024

STAINLESS STEEL WIRES

FDA Adverse Event
Death ·UNK·Product code GAQ·February 29, 2024

STAINLESS STEEL WIRES

FDA Adverse Event
Death ·UNK·Product code GAQ·February 29, 2024

PLATE

FDA Adverse Event
Death ·UNK·Product code HRS·February 29, 2024

NIPT (NON INVASIVE PREGNANCY TEST)

FDA Adverse Event
Malfunction ·COUNSYL·Product code MAO·May 21, 2016