280 results
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40ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
MAXENON XI 300
FDA Adverse Event
Malfunction
·QED, INC.·Product code FST·September 5, 2014
MAXENON XI 300
FDA Adverse Event
Malfunction
·QED, INC·Product code EQH·April 23, 2014
MAXENON XI 300
FDA Adverse Event
Malfunction
·QED INC·Product code FST·June 4, 2014
MAXENON XI 300-WATT XENON LIGHT SOURCE
FDA Adverse Event
Injury
·QED, INC·Product code FST·January 16, 2014
MAXENON XI 300-WATT XENON LIGHT SOURCE
FDA Adverse Event
Injury
·QED, INC·Product code FST·September 16, 2013
MAXENON XI 300-WATT XENON LIGHT SOURCE
FDA Adverse Event
Injury
·QED, INC·Product code GCT·September 16, 2013
MAXENON XI 300-WATT XENON LIGHT SOURCE
FDA Adverse Event
Injury
·QED, INC·Product code FST·September 16, 2013
NOVA 300 XENON
FDA Adverse Event
Malfunction
·QED MEDICAL, INC·Product code FST·March 1, 2013
ACCESSORIES FOR SPACE PUMPS
FDA Adverse Event
Malfunction
·B. BRAUN MELSUNGEN AG·Product code FRN·August 25, 2014
AED, INC.
FDA Adverse Event
Injury
·AES, INC.·Product code CAE·May 30, 2014
INFUSOMAT SPACE - US VERSION
FDA Adverse Event
Malfunction
·B. BRAUN MELSUNGEN AG·Product code FPA·August 25, 2014
DYNA MED INC.
FDA Adverse Event
Malfunction
·DYNA MED INC.·Product code HST·February 22, 2007
VIPER DISTAL VOLAR RADIUS PLATE IMPLANT
FDA Adverse Event
Other
·KINETIKOS MEDICAL, INC.·Product code HRS·January 27, 2006
UNIVERSAL TOTAL WRIST
FDA Adverse Event
Other
·KINETIKOS MEDICAL, INC.·Product code HRS·September 12, 2006
STEFFE PEDICLE SCREW
FDA Adverse Event
Injury
·MICRO MED, INC.·Product code MCV·June 13, 1995
MICROCLACE MED INC - HOSPIRA
FDA Adverse Event
Malfunction
·Product code FPA·July 23, 2010
MONOJECT SAFETY NDL 25 X 1
FDA Adverse Event
Malfunction
·CARDINAL HEALTH·Product code FMI·October 2, 2023
MONOJECT SAFETY NDL 25 X 1
FDA Adverse Event
Malfunction
·CARDINAL HEALTH·Product code FMI·November 30, 2023
BOSTON SCIENTIFIC SCI-MED INC
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC·Product code DQX·September 4, 2002
BRASSELER TRITON ALL IN ONE IRRIGATION SOLUTION
FDA Adverse Event
Injury
·INTER-MED, INC.·Product code KJJ·April 28, 2025