9 results
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73ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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FARADRIVE STEERABLE SHEATH CLEAR
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code DRA·February 12, 2026
XACT CAROTID STENT SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-VS·Product code NIM·December 13, 2010
PROMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code NIQ·January 21, 2011
ABBVIE PEG
FDA Adverse Event
Injury
·ABBVIE - MEDICAL DEVICE CENTER·Product code KNT·February 2, 2016
GRASPING FORCEPS
FDA Adverse Event
Injury
·OLYMPUS MEDICAL SYSTEMS CORP.·Product code EOQ·June 3, 2021
FARAWAVE
FDA Adverse Event
Injury
·FARAPULSE, INC.·Product code QZI·January 7, 2026
PROMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code NIQ·November 30, 2011
ENDEAVOR RX
FDA Adverse Event
Death
·MEDTRONIC IRELAND·Product code NIQ·September 26, 2012
SPYSCOPE DS ACCESS & DELIVERY CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - SPENCER·Product code FBN·May 31, 2018