10 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
NEOCIF INSERTION INSTRUMENT
FDA Adverse Event
Malfunction
·BIOMET SPAIN, S.L.·Product code MQP·November 6, 2018
NEOCIF INSERTION INSTRUMENT
FDA Adverse Event
Malfunction
·BIOMET SPAIN, S.L.·Product code MQP·July 20, 2017
TPRLOC COCR CMTD STM T1 12.5MM
FDA Adverse Event
Death
·BIOMET UK LTD.·Product code JDI·March 23, 2026
CMK MOD 12/14 SZ202 L130
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code LZO·November 24, 2025
PHILIPS INFORMATION CENTER
FDA Adverse Event
Death
·PHILIPS MEDICAL SYSTEMS·Product code MHX·April 29, 2013
COAGUCHEK ® XS SYSTEM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code GJS·September 16, 2014
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 27, 2011
MECTACER BIOLOX DELTA FEMORAL BALL HEAD
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·January 29, 2026
REVITAN, DISTAL PART, CURVED, UNCEMENTED, 24/200
FDA Adverse Event
Injury
·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code KWY·July 20, 2023
CMK MOD 12/14 SZ202 L130
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LZO·January 8, 2026