28 results
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37ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
GLENOID, PE WITH PEG, SMALL
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code KWS·January 2, 2019
USP II HUMERAL HEAD 44/19
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code KWS·January 2, 2019
UNIVERS APEX HUMERAL STEM, 10MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code KWS·January 2, 2019
GLENOID, PE WITH PEG, SMALL
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code KWS·April 1, 2020
GLENOID, PE WITH PEG, SMALL
FDA Adverse Event
Malfunction
·ARTHREX, INC.·Product code KWS·August 7, 2024
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
GLENOID, PE WITH PEG, SMALL
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code KWS·August 7, 2024
UNIVERS VAULTLOCK GLENOID, SMALL
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code KWS·January 2, 2019
USP II HUMERAL HEAD 46/20
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code KWS·January 2, 2019
BASIC LAP PACK
FDA Adverse Event
Malfunction
·DEROYAL INDUSTRIES, INC.·Product code FDE·March 21, 2024
REPLY
FDA Adverse Event
Injury
·SORIN BIOMEDICA CRM S.R.L.·Product code NVZ·November 18, 2010
INGENIO
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 2, 2014
5MM MONOPOLAR HANDLE 33CM
FDA Adverse Event
Malfunction
·STRYKER ENDOSCOPY SAN JOSE·Product code KOG·December 3, 2012
ARTHREX ECLIPSE HUMERAL HEAD, 43/16
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code QHQ·November 16, 2020
ECLIPSE CAGE SCREW M, 35MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code QHQ·November 16, 2020
ECLIPSE TRUNION,43 MM TPS CTD
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code QHQ·November 16, 2020
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
Injury
·ARTHREX, INC.·Product code KWS·December 5, 2022