8 results
·
39ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
TORQ STERNAL CLOSURE DEVICE
FDA Adverse Event
Malfunction
·KARDIUM INC.·Product code LXH·September 10, 2012
TORQ STERNAL CLOSURE DEVICE
FDA Adverse Event
Malfunction
·KARDIUM INC.·Product code LXH·April 1, 2010
ENDOPATH ETS COMPACT FLEX45 ENDOSCOPIC ARTICULATING
FDA Adverse Event
Injury
·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code GCJ·April 17, 2006
MOSES PULSE
FDA Adverse Event
Injury
·LUMENIS LTD·Product code GEX·May 28, 2026
XI 30 ENDOWRIST STAPLER
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL INC·Product code NAY·December 20, 2018
FLEXCATH ADVANCE STEERABLE SHEATH
FDA Adverse Event
Injury
·MEDTRONIC CRYOCATH LP·Product code DRA·February 1, 2024
ACHIEVE MAPPING CATHETER - 20 MM
FDA Adverse Event
Injury
·MEDTRONIC MEXICO S. DE R.L. DE CV·Product code DRF·February 1, 2024
MOSES PULSE
FDA Adverse Event
Injury
·LUMENIS LTD·Product code GEX·June 5, 2025