494 results · 26ms · Sources: EU EUDAMED, US FDA

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CNS-6201A

FDA Adverse Event
Malfunction ·NIHON KOHDEN CORPORATION·Product code MHX·February 10, 2020

ACRYSOF IQ TORIC

FDA Adverse Event
Injury ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·November 7, 2011

ACRYSOF IQ TORIC

FDA Adverse Event
Injury ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·November 7, 2011

SYNERGY

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO·Product code LGW·December 4, 2008

ASR ACETABULAR IMPLANT 56

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL·Product code KWA·September 16, 2011

ANIMAS VIBE

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·July 29, 2013

ACRYSOF RESTOR

FDA Adverse Event
Injury ·ALCON RESEARCH, LTD./HUNTINGTON·Product code MFK·March 25, 2011

PERMANENT PACEMAKER ELECTRODE

FDA Adverse Event
Malfunction ·MEDTRONIC·Product code DTB·August 12, 2023

INRATIO

FDA Adverse Event
Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·May 16, 2011

SPRINT FIDELIS

FDA Adverse Event
Malfunction ·MEDTRONIC·Product code LWS·August 11, 2023

PULSE GENERATOR, PERMANENT, IMPLANTABLE

FDA Adverse Event
Injury ·MEDTRONIC·Product code NVZ·August 12, 2023

ESPIRIT

FDA Adverse Event
Injury ·SORIN CRM S.R.L. - SALUGGIA - ITALY·Product code NVZ·March 25, 2011

ACRYSOF RESTOR

FDA Adverse Event
Injury ·ALCON RESEARCH, LTD./HUNTINGTON·Product code MFK·February 18, 2011

ACRYSERT DELIVERY SYSTEM

FDA Adverse Event
Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·June 22, 2011

UNKNOWN

FDA Adverse Event
Malfunction ·MEDTRONIC·Product code DTB·August 12, 2023

DRUG ELUTING PERMANENT RIGHT VENTRICULAR (RV) OR RIGHT ATRIAL (RA) PACEMAKER ELE

FDA Adverse Event
Malfunction ·MEDTRONIC·Product code NVN·August 12, 2023

RELOADABLE LINEAR CUTTER

FDA Adverse Event
Death ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·June 28, 2011

UNKNOWN

FDA Adverse Event
Malfunction ·MEDTRONIC·Product code DTB·August 12, 2023

PALINDROME RT 15FR 19CM KIT

FDA Adverse Event
Malfunction ·COVIDIEN·Product code MPB·April 5, 2011

REPLY

FDA Adverse Event
Malfunction ·SORIN C.R.M., S.R.L.·Product code NVZ·February 25, 2011