6 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
ESPRIT VENTILATOR
FDA Adverse Event
Malfunction
·RESPIRONICS CALIFORNIA, INC.·Product code CBK·June 18, 2014
BILIARY STENT, BILIARY STENT SYSTEM, BILIARY ENDOPROSTHESIS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - SPENCER·Product code FGE·October 25, 2010
SUTURE ANCHOR, PEEK SWIVELOCK C
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code MAI·December 20, 2012
ECHELON
FDA Adverse Event
Injury
·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·March 14, 2025
REFLEX CATHETER
FDA Adverse Event
Injury
·MICRO THERAPEUTICS, INC. DBA EV3·Product code DQY·March 14, 2025
VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAM·April 16, 2024