57 results · 72ms · Sources: EU EUDAMED, US FDA

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SANOFI-AVENTIS

FDA Adverse Event
Injury ·SANOFI-AVENTIS U.S.·Product code LMH·March 13, 2011

HYALGAN

FDA Adverse Event
Injury ·HYALGAN FIDIA FARMACEUTICI S.P.A.·Product code MOZ·June 15, 2011

SYNVISC ONE

FDA Adverse Event
Injury ·SANOFI - AVENTIS U.S. LLC·Product code MOZ·June 26, 2014

SCULPTRA

FDA Adverse Event
Injury ·SANOFI AVENTIS U.S. LLC·Product code LMH·April 12, 2010

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FDA Adverse Event
Malfunction ·SANOFI-AVENTIS U.S. LLC·Product code FMF·May 17, 2010

SCULPTRA (POLY-L-LACTIC ACID)

FDA Adverse Event
Injury ·SANOFI AVENTIS U.S. LLC·Product code LMH·April 12, 2010

DUPIXENT PEN INJECTOR (2-PKG)

FDA Adverse Event
Malfunction ·SANOFI-AVENTIS U.S. LLC.·Product code NSC·November 12, 2021

SYNVISC GEL INJECTION

FDA Adverse Event
Injury ·SANOFI-AVENTIS U.S. LLC·Product code MOZ·July 30, 2024

SCULPTRA

FDA Adverse Event
SANOFI AVENTIS U.S. LLC·Product code LMH·October 26, 2010

SCULPTRA (POLY L-LACTIC ACID)

FDA Adverse Event
Injury ·SANOFI-AVENTIS U.S. LLC·Product code LMH·December 2, 2009

SCULPTRA (POLY-L-LACTIC ACID)

FDA Adverse Event
Injury ·SANOFI-AVENTIS U.S. LLC·Product code LMH·December 2, 2009

SCULPTRA

FDA Adverse Event
Injury ·SANOFI AVENTIS U.S. LLC·Product code LMH·October 22, 2010

SCULPTRA (POLY-L-LACTIC ACID)

FDA Adverse Event
Injury ·SANOFI-AVENTIS, U.S. LLC·Product code LMH·October 22, 2010

POLY-L-LACTIC ACID (POLY-L-LACTIC ACID)

FDA Adverse Event
Injury ·SANOFI AVENTIS U.S. LLC·Product code LMH·October 22, 2010

SCULPTRA

FDA Adverse Event
Injury ·SANOFI AVENTIS U.S. LLC·Product code LMH·October 22, 2010

SCULPTRA (POLY-L-LACTIC ACID)

FDA Adverse Event
Injury ·SANOFI AVENTIS U.S. LLC·Product code LMH·October 22, 2010

SCULPTRA (POLY-L-LACTIC ACID)

FDA Adverse Event
Injury ·SANOFI AVENTIS U.S. LLC·Product code LMH·October 22, 2010

SCULPTRA

FDA Adverse Event
Injury ·SANOFI AVENTIS U.S. LLC.·Product code LMH·October 22, 2010

SCULPTRA

FDA Adverse Event
Injury ·SANOFI AVENTIS U.S. LLC·Product code LMH·October 22, 2010

SYNVISC-ONE VISCOSUPPLEMENT GEL

FDA Adverse Event
Death ·SANOFI-AVENTIS U.S. LLC·Product code MOZ·December 21, 2018