24 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
UNIVERSAL GLENOID - CENTRAL SCREW 20MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code PHX·February 26, 2024
FREESTYLE LITE
FDA Adverse Event
Malfunction
·Product code NBW·April 6, 2010
ECLIPSE CAGE SCREW S, 30MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code QHQ·December 16, 2019
ARTHREX ECLIPSE HUMERAL HEAD, 41/16
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code QHQ·December 16, 2019
ECLIPSE TRUNION,41 MM TPS CTD
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code QHQ·December 16, 2019
ARTHREX ECLIPSE HUMERAL HEAD, 41/16
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code QHQ·January 23, 2023
ECLIPSE CAGE SCREW M, 35MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code QHQ·January 23, 2023
UNIVERS VAULTLOCK GLENOID, SMALL
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code KWS·January 23, 2023
ARTHREX ECLIPSE HUMERAL HEAD, 41/16
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code QHQ·December 4, 2019
ECLIPSE TRUNION,41 MM TPS CTD
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code QHQ·December 4, 2019
ECLIPSE CAGE SCREW S, 30MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code QHQ·December 4, 2019
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 3, 2013
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 1, 2014
SOLYX SIS SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·December 21, 2010
GLENOID, PE WITH PEG, SMALL
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code KWS·December 4, 2019
GLENOID, PE WITH PEG, SMALL
FDA Adverse Event
Malfunction
·Product code KWS·April 5, 2021
ECLIPSE CAGE SCREW M, 35MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code QHQ·April 9, 2021
ECLIPSE TRUNION,41 MM TPS CTD
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code QHQ·April 9, 2021
ECLIPSE CAGE SCREW M, 35MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code QHQ·February 26, 2024
UNIVERS REVERS GLENOID
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code PHX·February 26, 2024