9 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
LACTOSORB SYSTEM 2.0 X 5 MM SUSPENSION PUSH SCREW
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code MBI·August 15, 2019
DIAMONDBACK 360 CORONARY ORBITAL ATHERECTOMY SYSTEM
FDA Adverse Event
Injury
·CARDIOVASCULAR SYSTEMS, INC.·Product code MCX·April 7, 2020
LACTOSORB CRANIOFACIAL ANCHOR-PUSH SCREW
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code DZL·November 21, 2014
TENDRIL ST
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code DTB·January 13, 2014
CAPSURE FIX NOVUS
FDA Adverse Event
Malfunction
·MEDTRONIC SINGAPORE OPERATIONS·Product code DTB·June 7, 2013
ACCESS 2 IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code JJE·June 24, 2011
LACTOSORB SYSTEM 2.0 X 5 MM SUSPENSION PUSH SCREW2-PACK
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code MBI·September 4, 2018
ADVANCE
FDA Adverse Event
Injury
·MEDTRONIC, INC·Product code DXE·September 9, 2019
TRUE METRIX
FDA Adverse Event
Malfunction
·TRIVIDIA HEALTH INC·Product code NBW·December 3, 2021