8 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
DIMENSION RXL MAX WITH HM
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS·Product code JJE·March 12, 2013
TDXFLX SYSTEM
FDA Adverse Event
Malfunction
·ABBOTT MANUFACTURING, INC.·Product code JJQ·February 24, 2011
GAMBRO CARTRIDGE BLOOD SET
FDA Adverse Event
Injury
·GAMBRO RENAL PRODUCTS S.A. DE C.V.·Product code FJK·February 20, 2008
EVIS EXERA III DUODENOVIDEOSCOPE
FDA Adverse Event
Injury
·AIZU OLYMPUS CO., LTD.·Product code FDT·October 1, 2024
INSORB 30 STAPLER
FDA Adverse Event
Injury
·COOPERSURGICAL, INC.·Product code GDW·November 1, 2023
BAXJECT II HI-FLOW NEEDLESS TRANSFER DEVICE
FDA Adverse Event
Malfunction
·TAKEDA PHARMACEUTICALS U.S.A., INC.·Product code LHI·May 4, 2026
INFUSE BONE GRAFT
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·February 27, 2024
CMD 20-1413 GLENOID IMPLANT
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A.·Product code KWS·March 11, 2022