20 results · 27ms · 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.

PENUMBRA SMART COIL

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code HCG·August 12, 2022

CARELINK

FDA Adverse Event
Malfunction ·MEDTRONIC MILACA INC.·Product code DXY·August 11, 2011

SHOULDER SYSTEM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code PHX·December 19, 2024

COATED VICRYL RAPIDE (POLYGLACTIN 910) SUTURE

FDA Adverse Event
Injury ·ETHICON, INC.·Product code GAM·March 14, 2013

UNKNOWN ZIMMER CR FLEX FEMORAL COMPONENT

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code JWH·February 24, 2011

NEXGEN COMPLETE KNEE SOLUTION FLEXION BALANCING INTRUMENTATION FEMORAL ANTERIOR/

FDA Adverse Event
Malfunction ·ZIMMER, INC.·Product code KWY·February 22, 2008

ENRHYTHM

FDA Adverse Event
Injury ·MDT PUERTO RICO OPERATIONS CO, MED REL·Product code NVZ·December 12, 2011

BIOMET TAPERLOC FEMORAL STEM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·March 5, 2018

TOTAL TEMPOROMANDIBULAR JOINT REPLACEMENT SYSTEM

FDA Adverse Event
Injury ·BIOMET MICROFIXATION·Product code LZD·August 4, 2016

TOTAL TEMPOROMANDIBULAR JOINT REPLACEMENT SYSTEM

FDA Adverse Event
Injury ·BIOMET MICROFIXATION·Product code LZD·August 4, 2016

TOTAL TEMPOROMANDIBULAR JOINT REPLACEMENT SYSTEM

FDA Adverse Event
Injury ·BIOMET MICROFIXATION·Product code LZD·August 4, 2016

BIOMET COCR FEMORAL HEAD

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·March 5, 2018

OPTIFLUX 180NR DIALYZER FINISHED ASSMBLY

FDA Adverse Event
Malfunction ·OGDEN MANUFACTURING PLANT·Product code KDI·July 21, 2018

IMPLANT MOUNT 3.4MM(D) X 15MM(L)

FDA Adverse Event
Malfunction ·BIOMET 3I·Product code NDP·April 26, 2019

OPTIFLUX 180NRE DIALYZER FINISHED ASSMBLY

FDA Adverse Event
Malfunction ·OGDEN MANUFACTURING PLANT·Product code KDI·August 13, 2018

OPTIFLUX 180NR DIALYZER FINISHED ASSMBLY

FDA Adverse Event
Malfunction ·OGDEN MANUFACTURING PLANT·Product code KDI·July 27, 2018

UNK OXFORD BEARING

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JWH·September 3, 2021

UNK OXFORD TIBIAL COMPONENT

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JWH·September 3, 2021

BIOMET RINGLOC+ ACETABULAR SHELL

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·February 7, 2018

BIOMET E1 POLY LINER

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code MAY·February 7, 2018