13 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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LIFEVEST WCD 4000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·February 11, 2013
PYRENEES CERVIAL PLATE
FDA Adverse Event
Injury
·K2M, INC.·Product code KWQ·February 23, 2011
PROXIMATE RELOADABLE LINEAR CUTTER WITH SAFETY LOCK-OUT
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code GDW·February 15, 2008
BD Q-SYTE¿ LUER ACCESS SPLIT-SEPTUM STAND-ALONE DEVICE
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·July 31, 2019
OXF UNI CMNTLS TIB SZ D RM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code NRA·August 31, 2021
OXF ANAT BRG RT MD SIZE 6 PMA
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code NRA·August 31, 2021
LIGHTSHEER EC
FDA Adverse Event
Injury
·RH USA, INC.·Product code GEX·August 28, 2012
DRILL 1.6X50MM 22MM STOP
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code HBE·July 28, 2016
Q-SYTE CLOSED LUER ACCESS DEVICE
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·November 13, 2020
BD Q-SYTE¿ LUER ACCESS SPLIT-SEPTUM STAND-ALONE DEVICE
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·July 8, 2022
BD Q-SYTE¿ LUER ACCESS SPLIT-SEPTUM STAND-ALONE DEVICE
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·March 7, 2018
OXF ANAT BRG LT MD SIZE 5 PMA
FDA Adverse Event
Death
·BIOMET UK LTD.·Product code NRA·August 5, 2020
OXFORD CEMENTLESS TIBIA C LM
FDA Adverse Event
Death
·BIOMET UK LTD.·Product code NRA·August 5, 2020