10,000 results · 78ms · 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.

EZ-IO POWER DRIVER

FDA Adverse Event
Malfunction ·VIDACARE·Product code FMI·October 21, 2015

CR PLUS TIB BEARING, VIT E, SZ 4, 9MM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code MBH·December 26, 2024

BD PYXIS¿ MEDSTATION¿ ES

FDA Adverse Event
Malfunction ·CAREFUSION 303, INC.·Product code BRY·May 26, 2026

HUANG INNER EAR SHUNT / ELS SHUNT

FDA Adverse Event
Malfunction ·E. BENSON HOOD LABORATORIES, INC.·Product code ESZ·August 28, 2020

PROSTHESIS ENDOLYMPHATIC - POLYCEL

FDA Adverse Event
Malfunction ·MEDTRONIC XOMED INC.·Product code ESZ·March 5, 2015

GENESIS II SPC F/E SZ GDE

FDA Adverse Event
Malfunction ·SMITH & NEPHEW, INC.·Product code MBH·April 27, 2021

GENESIS II SPC F/E SZ GDE

FDA Adverse Event
Malfunction ·SMITH & NEPHEW, INC.·Product code MBH·April 19, 2021

GENESIS II SPC F/E SZ GDE

FDA Adverse Event
Injury ·SMITH & NEPHEW, INC.·Product code MBH·November 5, 2020

GENESIS II SPC F/E SZ GDE

FDA Adverse Event
Malfunction ·SMITH & NEPHEW, INC.·Product code HRY·November 11, 2021

GENESIS II SPC F/E SZ GDE

FDA Adverse Event
Malfunction ·SMITH & NEPHEW, INC.·Product code HRY·July 30, 2022

GENESIS II SPC F/E SZ GDE

FDA Adverse Event
Malfunction ·SMITH & NEPHEW, INC.·Product code MBH·March 26, 2019

TRULIANT TIB IMP CR INS STD SZ 4, 11MM

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·April 23, 2024

BD PYXIS¿ MEDSTATION¿ ES

FDA Adverse Event
Malfunction ·CAREFUSION 303, INC.·Product code BRY·July 5, 2025

KNEE BALANCER THRD IM ROD

FDA Adverse Event
Malfunction ·SMITH & NEPHEW, INC.·Product code HRY·March 1, 2022

JOURNEY F/E GAP BAL SZ GDE

FDA Adverse Event
Malfunction ·SMITH & NEPHEW, INC.·Product code MBH·April 19, 2021

CR PLUS TIB BEARING, VIT E, SZ 1, 9MM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code MBH·May 10, 2024

CR PLUS TIB BEARING, VIT E, SZ 7, 14MM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code MBH·June 19, 2024

CR PLUS TIB BEARING, VIT E, SZ 1, 9MM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code MBH·May 10, 2024

CR PLUS TIB BEARING, VIT E, SZ 7, 8MM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code MBH·December 17, 2024

DJO SURGICAL

FDA Adverse Event
Injury ·ENCORE MEDICAL L.P.·Product code JWH·October 3, 2025