46 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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PRIMORIS HIP STEM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·August 5, 2016
PRIMORIS FEMORAL STEM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·October 3, 2017
PRIMORIS NECK PROSTH BM SZ 26
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·August 4, 2016
PRIMORIS HIP STEM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·August 5, 2016
PRMRS NCK STEM TI BM SZ 24 RSA
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·June 23, 2016
TAPERLOC LAT COCR 10MM T1
FDA Adverse Event
Death
·BIOMET UK LTD.·Product code JDI·March 20, 2026
TPRLOC COCR CMTD STEM T1 7.5MM
FDA Adverse Event
Death
·BIOMET UK LTD.·Product code JDI·March 20, 2026
UNKNOWN PRIMORIS HIP
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·August 4, 2016
PRMRS NCK STEM TI BM SZ 24 RSA
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code KWY·April 13, 2018
PRIMARY PLUMSET 2 CLAVES 272CM NDEHP
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·April 8, 2013
AED PLUS
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·April 4, 2011
ZEPHYR XL DR
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·May 27, 2008
PRIMORIS NECK PROSTHESIS TI BM SIZE 26
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·November 9, 2017
ENDOVIVE 3S LOW PROFILE BALLOON KIT
FDA Adverse Event
Malfunction
·XERIDIEM MEDICAL DEVICES·Product code PIF·January 20, 2016
UNKNOWN PRIMORIS HIP
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·August 4, 2016
UNKNOWN PRIMORIS HIP
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·August 5, 2016
PRMRS NCK STEM TI BM SZ 24 RSA
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·April 13, 2018
TPRLC COCR 10X140MM 12/14
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·March 20, 2026
PRMRS NCK STEM TI BM SZ 30 RSA
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LZO·April 10, 2018
PRMRS NCK STEM TI BM SZ 24 RSA
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·April 13, 2018