11 results
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29ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
PINNACLE SECTOR II CUP 54MM
FDA Adverse Event
Injury
·1818910 DEPUY ORTHOPAEDICS, INC.·Product code LPH·August 26, 2013
ARTICULEZE M HEAD 36MM +5
FDA Adverse Event
Injury
·8010379 DEPUY INTL., LTD.·Product code JDI·August 26, 2013
PINNACLE MTL INS NEUT36IDX54OD
FDA Adverse Event
Injury
·8010379 DEPUY INTL., LTD.·Product code KWA·August 26, 2013
KEEPSAFE DELUXE
FDA Adverse Event
Malfunction
·J. T. POSEY CO.·Product code KMI·December 7, 2012
INTEGRATED APD SET W/CASSETTE3-PRONG
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·December 4, 2010
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 4, 2014
SUMMIT POR TAPER SZ7 HI OFF
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·April 3, 2013
PINNACLE 100 ACET CUP 58MM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·April 3, 2013
PINNACLE MTL INS NEUT36IDX58OD
FDA Adverse Event
Malfunction
·DEPUY ORTHOPAEDICS INC US·Product code KWA·October 27, 2012
PINNACLE MTL INS NEUT36IDX56OD
FDA Adverse Event
Malfunction
·DEPUY ORTHOPAEDICS INC US·Product code KWA·October 27, 2012
ARTICULEZE M HEAD 36MM +5
FDA Adverse Event
Malfunction
·DEPUY ORTHOPAEDICS INC US·Product code JDI·October 27, 2012