6 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
UNIVERS APEX HUMERAL STEM, SIZE 5
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code KWS·September 24, 2025
UNIVERSAL QC HEX DRIVER
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code HXX·July 15, 2015
PRECISION XTRA
FDA Adverse Event
Malfunction
·Product code NBW·January 14, 2013
ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK INSTRUMENT MANUFACTURING·Product code LXH·December 3, 2010
UNIVERS VAULTLOCK GLENOID, SMALL
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code KWS·October 1, 2025
UNIVERS HUMERAL HEAD 45/15
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code KWS·October 1, 2025