10,000 results
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55ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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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