1,757 results
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36ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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ATELLICA CH 930 ANALYZER
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JJE·June 23, 2020
UNKNOWN M/L TAPER STEM
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code KWA·February 3, 2017
UNKNOWN 32MM HEAD
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code KWY·January 31, 2017
UNKNOWN ML TAPER STEM
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code KWA·January 31, 2017
CARDIOSAVE HYBRID, 3.1 EDITION
FDA Adverse Event
Malfunction
·DATASCOPE CORP. - MAHWAH·Product code DSP·April 28, 2023
BD SEDI-40
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code GHC·June 12, 2018
TVT-S
FDA Adverse Event
Injury
·JNJ·Product code FTL·November 15, 2008
CARDIOSAVE HYBRID, TYPE B PLUG
FDA Adverse Event
Malfunction
·DATASCOPE CORP. - MAHWAH·Product code DSP·July 18, 2023
BD INSYTE AUTOGUARD
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FOZ·April 26, 2024
UNSPECIFIED BD SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMF·September 15, 2022
EUFLEXXA INJ
FDA Adverse Event
Injury
·UNK·Product code MOZ·November 2, 2017
PEN INJ
FDA Adverse Event
Injury
·ELI LILLY AND COMPANY PHARMACEUTICAL DELIVERY SYSTEMS·Product code FMF·October 11, 2018
ORTHOVISC INJ
FDA Adverse Event
Injury
·ANIKA THERAPEUTICS INC.·Product code MOZ·April 30, 2019
MONOVISC INJ
FDA Adverse Event
Injury
·ANIKA THERAPEUTICS, INC.·Product code MOZ·January 24, 2020
UNSPECIFIED BD¿ PEN NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMI·August 8, 2023
UNSPECIFIED BD¿ PEN NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMI·October 12, 2023
UNSPECIFIED BD POSIFLUSH¿ SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code NGT·June 14, 2023
SZ 32 MM PINNACLE ALTRX POLYETHYLENE ACETABULAR
FDA Adverse Event
Injury
·JNJ DEPUY ORTHOPEDICS·Product code LPH·July 19, 2011
UNSPECIFIED BD PMCF-Q-SYTE-EXTENSION-SET
FDA Adverse Event
Injury
·BECTON DICKINSON·Product code FPA·April 14, 2021
CARDIOSAVE HYBRID, TYPE B PLUG
FDA Adverse Event
Malfunction
·DATASCOPE CORP. - MAHWAH·Product code DSP·July 3, 2024