6,643 results · 52ms · Sources: EU EUDAMED, US FDA

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COULTER® HMX HEMATOLOGY ANALYZER WITH AUTOLOADER

FDA Adverse Event
Malfunction ·BECKMAN COULTER·Product code GKZ·May 1, 2014

HYDRELLE

FDA Adverse Event
Other ·ANIKA THERAPEUTICS, INC.·Product code LMH·June 2, 2010

BD INSULIN SYRINGE WITH THE BD ULTRA-FINE¿ NEEDLE

FDA Adverse Event
Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·November 27, 2017

VOLIFT (VOLUME UNKNOWN)

FDA Adverse Event
Injury ·ALLERGAN (PRINGY)·Product code LMH·June 30, 2021

SHUNT SENSOR SYS500

FDA Adverse Event
Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·October 1, 2014

SHUNT SENSOR SYS500

FDA Adverse Event
Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·April 3, 2012

COULTER® HMX HEMATOLOGY ANALYZER WITH AUTOLOADER

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·February 9, 2012

UNICEL DXC 600 SYNCHRON SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER·Product code JJE·September 8, 2015

CELLENTRA 10CC ADVANCED ALLOGRAFT

FDA Adverse Event
Malfunction ·EBI, LLC.·Product code MQV·July 14, 2015

EXTENSION SET 20 IN STERILE PACK

FDA Adverse Event
Malfunction ·ABBOTT LABORATORIES·Product code FPA·October 16, 2003

SYNCHROMED II

FDA Adverse Event
Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·November 17, 2014

BELOTERO BALANCE

FDA Adverse Event
Injury ·MERZ NORTH AMERICA·Product code LMH·August 12, 2015

VOLLURE (VOLUME UNKNOWN)

FDA Adverse Event
Injury ·PRINGY·Product code LMH·September 11, 2024

SOL-M

FDA Adverse Event
Malfunction ·SOL-MILLENNIUM MEDICAL INC·Product code FMI·December 10, 2025

REALIZE ADJ GASTRIC BAND-C

FDA Adverse Event
Injury ·OBTECH MEDICAL SARL_·Product code LTI·March 20, 2013

BD ULTRA-FINE¿ II INSULIN SYRINGE

FDA Adverse Event
Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·December 17, 2018

BD INSULIN SYRINGE WITH THE BD ULTRA-FINE¿ NEEDLE

FDA Adverse Event
Malfunction ·BD MEDICAL - DIABETES CARE·Product code FMF·December 14, 2018

SARNS CENTRIFUGAL PUMP

FDA Adverse Event
Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code KFM·March 7, 2013

HYDROTHERMABLATOR PROCEDURE SET

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MNB·December 12, 2008

SHUNT SENSOR SYS500

FDA Adverse Event
Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·February 14, 2014