22 results
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37ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Injury
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P150048
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code LWR·September 23, 2024
P150048
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code LWR·September 26, 2025
INCEPTA
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·April 10, 2013
SPRINT FIDELIS
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·May 8, 2008
FEMORAL STEM 12/14 NECK TAPER STANDARD OFFSET SIZE 1 130 MM STEM LENGTH
FDA Adverse Event
Injury
·ZIMMER MANUFACTURING B.V.·Product code JDI·August 23, 2019
TISSUE HEART VALVE
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code LWR·September 11, 2020
SEE. H10.
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code LWR·December 1, 2020
REPLACEMENT HEART VALVE
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·November 13, 2020
REPLACEMENT HEART VALVE
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code LWR·May 29, 2019
SEE H11
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·February 27, 2025
OPTIPAC-S 60 REFOBACIN BONE CEMENT R
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code MBB·September 2, 2019
AVANTAGE INSERT 48/22
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code LPH·August 30, 2019
OPTIPAC-S 60 REFOBACIN BONE CEMENT R
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code MBB·August 30, 2019
OPTIPAC-S 60 REFOBACIN BONE CEMENT R
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code MBB·December 18, 2019
AVANTAGE CEMENTED SHELL SS Ø48MM
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code JDI·August 30, 2019
OPTIPAC-S 60 REFOBACIN BONE CEMENT R
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code MBB·December 18, 2019
EDWARDS PERICARDIAL AORTIC BIOPROSTHESIS
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code LWR·September 27, 2024
FEMORAL STEM 12/14 NECK TAPER STANDARD OFFSET SIZE 1 130 MM STEM LENGTH
FDA Adverse Event
Injury
·ZIMMER MANUFACTURING B.V.·Product code JDI·August 22, 2019
FEMORAL HEAD STERILE PRODUCT DO NOT RESTERILIZE 12/14 TAPER
FDA Adverse Event
Injury
·ZIMMER MANUFACTURING B.V.·Product code LPH·August 23, 2019
AVANTAGE INLAY S48 / 22,2
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code LPH·August 30, 2019