9 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
S-ROM*SLEEVE PRX ZTT, 16D-LRG
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·December 12, 2013
PINNACLE 100 ACET CUP 54MM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·December 12, 2013
S-ROM M HEAD 36MM +0
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·December 12, 2013
S-ROM*STM STD,36NK,16X11X150
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JDI·December 12, 2013
PINNACLE MTL INS NEUT36IDX54OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code KWA·December 12, 2013
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·March 26, 2025
EXPEDIUM DI FINAL TIGHTENER
FDA Adverse Event
Malfunction
·DEPUY SYNTHES SPINE·Product code HWR·April 22, 2013
TAPERED SPACER ARTICUL/EZE -3
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code LZY·April 15, 2011
CONTOUR TEST STRIPS (50)
FDA Adverse Event
Malfunction
·BAYER HEALTHCARE, LLC.·Product code NBW·July 3, 2008