6 results
·
15ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code KWP·November 15, 2013
PH3 HEAD (03-3020-01)
FDA Adverse Event
Malfunction
·THEKEN SPINE·Product code NKB·December 22, 2010
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·April 3, 2013
BD DTX PLUS
FDA Adverse Event
Malfunction
·BECTON DICKINSON CRITICAL CARE SYSTEMS PTE LTD.·Product code DRS·April 22, 2008
REF H10
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code MMI·August 9, 2016
ATELLICA IM HIGH-SENSITIVITY TROPONIN I (TNIH)
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code MMI·December 10, 2020