10,000 results · 55ms · Sources: EU EUDAMED, US FDA

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DIGOXIN

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code KXT·March 15, 2024

DIGOXIN

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code KXT·March 7, 2024

VANCOMYCIN TEST SYSTEM

FDA Adverse Event
Malfunction ·SERADYN·Product code LEH·December 18, 2007

COBAS AMPLIPREP/COBAS TAGMAN CMV TEST

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code PAB·June 1, 2015

VACUETTE® TUBE 4 ML K2E K2EDTA 13X75

FDA Adverse Event
Malfunction ·GREINER BIO-ONE NA INC.·Product code JKA·December 15, 2022

ATELLICA IM CARCINOEMRYOINIC (CEA)

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code DHX·January 11, 2021

ADVIA CENTAUR XP PSA ASSAY

FDA Adverse Event
Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code MTF·July 5, 2018

MCGHAN

FDA Adverse Event
Injury ·MCGHAN·Product code FTR·July 25, 2000

PHARMCHEK SWAET PATCH

FDA Adverse Event
Injury ·PHARMCHEM, INC.·Product code FMH·August 26, 2025

IFORIA 3 DR-T DF-1

FDA Adverse Event
Malfunction ·BIOTRONIK SE & CO. KG·Product code MRM·May 3, 2021

ITREVIA 7 VR-T DX DF-1 PROMRI

FDA Adverse Event
Malfunction ·BIOTRONIK SE & CO. KG·Product code LWS·May 3, 2021

COBAS C 503 ANALYTICAL UNIT

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·February 16, 2023

ELECSYS FT4 IV

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code CEC·October 30, 2023

IMPELLA RP FLEX

FDA Adverse Event
Injury ·ABIOMED, INC.·Product code PYX·March 31, 2025

ELECSYS ESTRADIOL III

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code CHP·October 24, 2024

IFORIA 5 VR-T DX PROMRI DF-1

FDA Adverse Event
Malfunction ·BIOTRONIK SE & CO. KG·Product code LWS·October 6, 2020

INLEXA 3 VR-T DF-1

FDA Adverse Event
Malfunction ·BIOTRONIK SE & CO. KG·Product code LWS·October 8, 2020

ELECSYS VITAMIN D TOTAL III

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code MRG·December 8, 2025

BIOZORB

FDA Adverse Event
Injury ·HOLOGIC, INC·Product code NEU·September 5, 2023

BD VACUTAINER® PPT¿ PLASMA PREPARATION TUBE K2E 9.0 MG

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code PJE·May 12, 2023