6 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
AMIS MOBILE LEG POSITIONER
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL, SA·Product code FWX·March 6, 2014
BD NEXIVA¿ CLOSED IV CATHETER SYSTEM
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FOZ·March 8, 2018
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·May 14, 2013
ENTERRA
FDA Adverse Event
Injury
·MPROC, JUNCOS·Product code LNQ·August 13, 2008
ARTICULEZE M HEAD 36MM +1.5
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code JDI·May 13, 2011
ATELLICA IM HIGH-SENSITIVITY TROPONIN I (TNIH)
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code MMI·December 10, 2020