10 results
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29ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
FLOEY CATHETER W TEMP
FDA Adverse Event
Injury
·DEGANIA SILICONE LTD·Product code DRF·October 17, 2017
FOLEY CATHETER W TEMP
FDA Adverse Event
Malfunction
·DEGANIA SILICONE LTD.·Product code DRF·August 10, 2017
FOLEY CATHETER W TEMP
FDA Adverse Event
Malfunction
·DEGANIA SILICONE LTD.·Product code DRF·August 10, 2017
TORQUE WRENCH
FDA Adverse Event
Malfunction
·DEPUY SPINE INC·Product code HXC·April 2, 2021
FOLEY CATHETER W TEMP
FDA Adverse Event
Malfunction
·DEGANIA SILICONE LTD.·Product code KOD·July 7, 2017
IMMAGE® 800 IMMUNOCHEMISTRY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·November 14, 2012
PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code LWP·June 10, 2015
MAXCEM ELITE
FDA Adverse Event
Injury
·KERR CORPORATION·Product code EMA·September 10, 2010
FOLEY CATHETER W TEMP
FDA Adverse Event
Malfunction
·MMJ SA DE CV (USD)·Product code DRF·November 9, 2018
TORQUE WRENCH
FDA Adverse Event
Malfunction
·DEPUY SPINE INC·Product code HXC·September 9, 2024