8 results
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37ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
0009613348-2024-011592
FDA Adverse Event
Injury
·INSTITUT STRAUMANN AG·Product code DZE·September 2, 2024
EMERGE¿
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LOX·March 19, 2013
4 MOTOR ADVANCE BED
FDA Adverse Event
Malfunction
·HILL-ROM INC.·Product code FNL·February 14, 2011
*
FDA Adverse Event
Malfunction
·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code JTC·February 12, 2008
BD VACUTAINER® PST¿ GEL AND LITHIUM HEPARINN (LH) BLOOD COLLECTION TUBE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code JKA·June 19, 2018
BD VACUTAINER® PST¿ GEL LITHIUM HEPARINN BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code JKA·June 21, 2018
MOBILE LINER ØINT 28 MM Ø40 MM
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A.·Product code LZO·October 21, 2022
ACTIVA
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·October 9, 2020