133 results · 43ms · Sources: EU EUDAMED, US FDA

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ABBOTT AXSYM SYSTEM

FDA Adverse Event
Other ·ABBOTT MFG, INC.·Product code JJE·January 16, 1998

ARCHITECT C80000

FDA Adverse Event
Other ·ABBOTT MFG, INC.·Product code JJE·January 17, 2008

ABBOTT AXSYM SYSTEM

FDA Adverse Event
Other ·ABBOTT MANUFACTURING, INC.·Product code JJE·April 23, 1998

ABBOTT AXSYM SYSTEM

FDA Adverse Event
Other ·ABBOTT MFG., INC.·Product code JJE·March 2, 1998

IMX ANALYZER

FDA Adverse Event
Other ·ABBOTT MANUFACTURING, INC.·Product code JHI·August 4, 2003

CLINICAL CHEMISTRY PHENYTOIN

FDA Adverse Event
Other ·ABBOTT MANUFACTURING, INC.·Product code LES·November 8, 2007

V-CATH PICC

FDA Adverse Event
Other ·HDC CORP.·Product code DQO·December 24, 1996

2.0X0.6 2/2 HOLE LEFT MED L PLATE

FDA Adverse Event
Other ·BIOMET MICROFIXATION·Product code JEY·June 30, 2008

PERLANE-L INJECTABLE GEL

FDA Adverse Event
Other ·Q-MED AB·Product code LMH·July 2, 2012

ABBOTT AXSYM SYSTEM

FDA Adverse Event
Other ·ABBOTT MFG., INC.·Product code JJE·June 18, 1997

ARCHITECT C8000

FDA Adverse Event
Other ·ABBOTT MANUFACTURING, INC·Product code JJE·December 18, 2006

ALCON OPHTHALAS LASER

FDA Adverse Event
Other ·ALCON LABORATORIES·Product code HQF·June 21, 1996

SCULPTRA

FDA Adverse Event
Other ·GLOBAL PHARMACOVIGILANCE AND EPIDEMIOLOGY/SANOFI-AVENTIS·Product code LMH·April 18, 2007

2.0/0.6 2/2 HOLE RIGHT MED L PLATE

FDA Adverse Event
Other ·BIOMET MICROFIXATION·Product code JEY·September 10, 2008

ACCESS IMMUNOASSAY SYSTEM

FDA Adverse Event
Other ·BECKMAN COULTER, INC.·Product code JJE·November 15, 2002

SYNVISC (HYLAN G-F 20) INJECTION

FDA Adverse Event
Other ·GENZYME BIOSURY (RIDGEFIELD)·Product code MOZ·October 16, 2008

HUMAPEN ERGO, BURGUNDY/CLEAR

FDA Adverse Event
Other ·ELI LILLY AND CO·Product code KZE·December 21, 2006

NCB PP PROX FEM PLATE, L, 18 H, L. 363 MM

FDA Adverse Event
Other ·ZIMMER GMBH·Product code HRS·July 7, 2015

SCULPTRA

FDA Adverse Event
Other ·GLOBAL PHARMACOVIGILANCE AND EPIDEMIOLOGY/SANOFI-AVENTIS·Product code LMH·April 30, 2009

HUMAPEN ERGO 3 ML

FDA Adverse Event
Other ·ELI LILLY AND CO.·Product code KZE·September 7, 2001