12 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
CERTAIN GOLD-TITE TM HEXED SCREW
FDA Adverse Event
Malfunction
·BIOMET 3I·Product code NHA·April 3, 2025
M SERIES
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·November 13, 2008
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·September 15, 2011
HS III PROXIMAL SEAL SYSTEM 3.8MM
FDA Adverse Event
Injury
·MAQUET CARDIOVASCULAR, LLC·Product code DXC·July 24, 2013
QDOT MICRO
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code OAE·May 27, 2026
QDOT MICRO
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code OAE·April 28, 2026
QDOT MICRO
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code OAE·May 19, 2026
NGEN RF GENERATOR
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code OAE·December 16, 2025
NGEN RF GENERATOR, JAPAN
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code LPB·April 21, 2023
VERSAPORT PLUS
FDA Adverse Event
Malfunction
·DAVIS & GECK CARIBE LTD·Product code GCJ·December 12, 2022
QDOT MICRO
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code OAE·March 6, 2026
QDOT MICRO
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code OAE·February 6, 2026