9,434 results
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39ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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COMPLETE SE ILIAC
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code NIO·November 5, 2014
PIPELINE
FDA Adverse Event
Injury
·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·April 29, 2024
PIPELINE
FDA Adverse Event
Malfunction
·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·April 29, 2024
OLYMPUS AU400 CLINICAL CHEMISTRY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER MISHIMA K.K.·Product code JJE·December 6, 2011
COMPLETE SE ILIAC
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code NIO·November 5, 2014
UNICEL® DXC 600 SYNCHRON® SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·September 28, 2011
ZIMMER HIP IMPLANT
FDA Adverse Event
Injury
·ZIMMER·Product code KWA·February 28, 2017
CLOSED APHERESIS KIT, PL3014, SAMPLE POUCH AMS
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORP.·Product code GKT·April 8, 1997
COMPLETE SE ILIAC
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code NIO·November 5, 2014
COMPLETE SE ILIAC
FDA Adverse Event
Death
·MEDTRONIC IRELAND·Product code NIO·November 5, 2014
COMPLETE SE ILIAC
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code NIO·November 5, 2014
ASR ACETABULAR CUPS 56
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·June 29, 2012
HORIZON TI ML 6/CART 120/BOX
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code FZP·March 26, 2026
ASR UNI FEMORAL IMPL SIZE 47
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·November 28, 2011
ASR ACETABULAR CUPS 54
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·November 28, 2011
ACCU-CHEK ® COMPACT PLUS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code NBW·February 26, 2010
UNKNOWN HIP FEMORAL STEM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code KWA·April 27, 2021
HOMECHOICE PRO
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·November 30, 2012
COBAS INTEGRA 800
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JGS·October 13, 2009
UNKNOWN DEPUY ASR FEMORAL HEAD
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·March 12, 2012