8 results
·
25ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
SABRATEK TUBING (SABRA SET)
FDA Adverse Event
Malfunction
·SABRATEK CORP/BAXTER·Product code FPA·February 12, 2001
CD HORIZON® SPINAL SYSTEM
FDA Adverse Event
Malfunction
·Product code KWP·November 2, 2021
CD HORIZON® SPINAL SYSTEM
FDA Adverse Event
Malfunction
·Product code KWP·November 2, 2021
CD HORIZON® SPINAL SYSTEM
FDA Adverse Event
Malfunction
·Product code KWP·November 2, 2021
7700
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·February 12, 2013
XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code NIQ·February 25, 2011
CARPENTIER-MCCARTHY-ADAMS IMR ETLOGIX ANNUPLASTY RING
FDA Adverse Event
Death
·EDWARDS LIFESCIENCES·Product code KRH·February 18, 2008
OXYSEPT
FDA Adverse Event
Injury
·AMO(HANGZHOU) CO., LTD.·Product code LPN·July 8, 2024