7 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
HYDRATOME
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code KNS·March 29, 2007
PROMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·ABBOTT VASCULAR CLONMEL·Product code NIQ·June 18, 2010
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·ABBOTT VASCULAR·Product code MGB·June 27, 2022
STARTER GUIDEWIRE
FDA Adverse Event
Malfunction
·LAKE REGION MEDICAL LIMITED·Product code DQX·May 5, 2026
HEARTMATE II SYSTEM CONTROLLER
FDA Adverse Event
Malfunction
·THORATEC CORP.·Product code DSQ·May 9, 2013
SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
FDA Adverse Event
Injury
·BAXTER HEATHCARE CORPORATION·Product code FKX·September 26, 2014
SIG MOD TIB TRAY CEM COCR 3
FDA Adverse Event
Injury
·DEPUY-CORK, A DIVISION OF DEPUY ORTHOPAEDICS·Product code JWH·June 2, 2011