6 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
SMR GLENOID BASEPLATE STANDARD
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A.·Product code KWS·June 29, 2022
SINGLE USE DISTAL COVER
FDA Adverse Event
Injury
·OLYMPUS MEDICAL SYSTEMS CORP. HINODE PLANT·Product code FDT·October 16, 2024
HEARTMATE II LVAS
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·March 12, 2013
MEDTRONIC ANEURX STENT GRAFT SYSTEM
FDA Adverse Event
Death
·MEDTRONIC CARDIOVASCULAR·Product code MIH·February 18, 2011
PUMP MMT-715NAB PRDGM INS V2.1 BL EN
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code LZG·February 21, 2008
BAXJECT II HI-FLOW NEEDLESS TRANSFER DEVICE
FDA Adverse Event
Malfunction
·TAKEDA PHARMACEUTICALS U.S.A., INC.·Product code LHI·May 4, 2026