20 results · 31ms · 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.

VIDAS RUB IGG II 60 TESTS

FDA Adverse Event
Malfunction ·BIOMERIEUX SA·Product code LFX·April 3, 2020

ESSURE

FDA Adverse Event
Injury ·CONCEPTUS·Product code HHS·February 12, 2014

ESSURE

FDA Adverse Event
Injury ·CONCEPTUS·Product code HHS·February 12, 2014

MEDSTONE LITHOTRIPTOR

FDA Adverse Event
Malfunction ·HEALTHTRONICS, INC.·Product code LNS·June 12, 2017

OT VERIO METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 19, 2013

BHR

FDA Adverse Event
Injury ·SMITH & NEPHEW ORTHOPAEDICS, LTD.·Product code NXT·March 8, 2011

LIFEPAK 500 AUTOMATED EXTERNAL DEFIBRILLATOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·March 10, 2008

MICRUS MICROCOIL SYSTEM

FDA Adverse Event
Injury ·MICRUS ENDOVASCULAR CORPORATION·Product code MJN·February 10, 2012

BD SYRINGE 50ML LL

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·May 14, 2021

450 SAL EJECTOR 3283

FDA Adverse Event
Malfunction ·COVIDIEN·Product code DYN·June 23, 2016

UNKNOWN KNEE PATELLA

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·December 3, 2019

UNKNOWN KNEE FEMORAL

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·December 3, 2019

BD PLASTIPAK 50ML CONCENTRIC LUER LOCK SYRINGE

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·April 15, 2021

METAL METAL BALL HEAD 28L CONE

FDA Adverse Event
Injury ·SMITH & NEPHEW ORTHOPAEDICS AG·Product code LPH·April 15, 2022

ULTRA SHORT STRUT TL-HEX - 45MM-101MM

FDA Adverse Event
Injury ·ORTHOFIX SRL·Product code KTT·April 4, 2017

ULTRA SHORT STRUT TL-HEX - 45MM-101MM

FDA Adverse Event
Injury ·ORTHOFIX SRL·Product code KTT·April 27, 2016

VIDAS RUB IGG II 60 TESTS - 30221

FDA Adverse Event
Malfunction ·BIOMÉRIEUX, SA·Product code LFX·March 19, 2020

ULTRA SHORT STRUT TL-HEX - 45MM-101MM

FDA Adverse Event
Malfunction ·ORTHOFIX SRL·Product code KTT·September 21, 2016

MODULAR 5/8 RING, 160MM, TL-HEX

FDA Adverse Event
Injury ·ORTHOFIX SRL·Product code KTT·April 27, 2016

BICON-PLUS PE INSERT ANTIL 3/28 NON-CEM

FDA Adverse Event
Injury ·SMITH & NEPHEW ORTHOPAEDICS AG·Product code JDG·March 20, 2022