14 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
UNITRAY A LOCUS SSP
FDA Adverse Event
Malfunction
·Product code MZI·September 26, 2013
APEX MONORAIL
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code LOX·June 19, 2009
APEX MONORAIL
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code LOX·June 8, 2009
AS COLUMBUS CR FEMORAL COMP.CEMENTED F4R
FDA Adverse Event
Death
·AESCULAP AG·Product code JWH·October 5, 2022
A LOCUS SSP UNITRAY KIT
FDA Adverse Event
Malfunction
·LIFE TECHNOLOGIES CORPORATION·Product code MZI·December 26, 2013
MAVERICK2 MONORAIL PTCA CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code LOX·April 19, 2007
APEX MONORAIL
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code LOX·April 20, 2009
SELECTSECURE
FDA Adverse Event
Injury
·MPRI·Product code NVN·June 10, 2014
IAB: 8 FR - 40 CC
FDA Adverse Event
Malfunction
·ARROW INTL., INC.·Product code DSP·December 4, 2012
SYNCHRON CX9 ALX
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJC·October 7, 2010
CATHETERS, TRANSLUMINAL CORONARY ANGIOPLASTY, PERCUTANEOUS
FDA Adverse Event
Death
·BOSTON SCIENTIFIC·Product code MAF·June 20, 2007
G7 SCREW 6.5MM X 35MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code PBI·July 22, 2025
G7 SCREW 6.5MM X 20MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code PBI·July 22, 2025
G7 OSSEOTI 3 HOLE SHELL 50MM D
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·July 22, 2025