10,000 results · 72ms · Sources: EU EUDAMED, US FDA

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EVOLUT FX VALVE

FDA Adverse Event
Malfunction ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·January 8, 2025

LP COIL SYSTEM

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code HCG·July 31, 2023

EVOLUT FX VALVE

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·July 2, 2024

CLICKLINE

FDA Adverse Event
Malfunction ·KARL STORZ ENDOSCOPY-AMERICA, INC.·Product code GCJ·September 29, 2009

CARPENTIER-EDWARDS PERIMOUNT MAGNA AORTIC BIOPROSTHESIS

FDA Adverse Event
Injury ·EDWARDS LIFESCIENCES·Product code LWR·November 21, 2008

ARTHREX

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code MBI·April 18, 2023

REAL INTELLIGENCE ROBOTIC DRILL

FDA Adverse Event
Malfunction ·BLUE BELT TECHNOLOGIES·Product code OLO·February 20, 2024

GAP SPOON-1MM-2MM

FDA Adverse Event
Malfunction ·MAKO SURGICAL CORP.·Product code OLO·November 18, 2019

ALCON CLAREON INTRA-OCULAR LENS

FDA Adverse Event
Malfunction ·ALCON LABORATORIES IRELAND LTD.·Product code HQL·September 26, 2022

PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM

FDA Adverse Event
Malfunction ·NUVASIVE, INC.·Product code HSB·September 30, 2025

VALLEY LAB

FDA Adverse Event
Injury ·VALLEYLAB, INC.·Product code GEI·November 22, 1994

ROMEO 2 INSTRUMENTATION

FDA Adverse Event
Malfunction ·SPINEART SA·Product code MNH·October 18, 2021

UNKNOWN LCCK FEMORAL COMPONENT

FDA Adverse Event
Injury ·ZIMMER INC·Product code JWH·December 8, 2015

BD ECLIPSE¿ NEEDLE

FDA Adverse Event
Malfunction ·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code FMI·August 11, 2023

1X HUNT TROCAR 5MM PYRAMIDAL TIP

FDA Adverse Event
Malfunction ·APPLE MEDICAL CORPORATION·Product code GCJ·March 21, 2002

DEPUY DELTA EXTEND

FDA Adverse Event
Malfunction ·DEPUY ORTHOPEDICS·Product code KWS·November 4, 2011

ELEKTA MEDICAL LINEAR ACCELERATOR

FDA Adverse Event
Malfunction ·ELEKTA SOLUTIONS AB·Product code IYE·May 17, 2023

CONMED ELECTROSURGICAL ACTIVE INSTRUMENT

FDA Adverse Event
Malfunction ·CONMED CORPORATION·Product code GEI·March 21, 1997

KOMPRESSOR MINI COMPRESSION DRIVER

FDA Adverse Event
Malfunction ·INTEGRA LIFESCIENCES CORPORATION·Product code HWC·December 9, 2008

COREVALVE 29MM AORTIC VALVE

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·January 2, 2015