9 results
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21ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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LEGACY3 IMPLANT
FDA Adverse Event
Malfunction
·IMPLANT DIRECT SYBRON MANUFACTURING LLC·Product code DZE·August 15, 2018
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·June 6, 2014
CANNULATED SCREW
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code HWC·December 3, 2012
TERUMO CDI 500 BLOOD PARAMETER MONITOR
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·September 3, 2010
ATTUNE MEDIAL DOME PAT 32MM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JWH·December 11, 2024
ATTUNE CR FEM LT SZ 3 CEM
FDA Adverse Event
Injury
·DEPUY IRELAND - 9616671·Product code JWH·December 11, 2024
HP STRL THREADED PINS HEADED
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LXH·December 11, 2024
ATTUNE FB TIB BASE SZ 3 CEM
FDA Adverse Event
Injury
·DEPUY IRELAND - 9616671·Product code JWH·December 11, 2024
PROTECT SLEEVE 11/8 GREEN
FDA Adverse Event
Malfunction
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code LXH·November 1, 2019