12 results
·
35ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
2031527-2012-00108
FDA Adverse Event
Malfunction
·ENDOLOGIX, INC.·October 29, 2012
AFX
FDA Adverse Event
Malfunction
·ENDOLOGIX INC.·Product code MIH·October 12, 2016
HOMECHOICE PRO
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·April 2, 2013
ADVANTAGE SERIES 26 OBS
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FPO·March 21, 2011
ELIMINATOR ICW
FDA Adverse Event
Malfunction
·ARTHROCARE CORP.·Product code GEI·March 11, 2020
POWERLINK SYSTEM
FDA Adverse Event
Malfunction
·ENDOLOGIX, INC.·Product code MIH·October 24, 2006
POWERLINK SYSTEM
FDA Adverse Event
Malfunction
·ENDOLOGIX, INC.·Product code MIH·February 1, 2008
AFX SYSTEM
FDA Adverse Event
Malfunction
·ENDOLOGIX, INC.·Product code MIH·September 11, 2012
IMPL TAPERED SCR-V SBM 3.7MM 3.5MM 13MM
FDA Adverse Event
Malfunction
·ZIMMER DENTAL·Product code DZE·April 9, 2019
AFX SYSTEM
FDA Adverse Event
Malfunction
·ENDOLOGIX, INC.·Product code MIH·December 21, 2012
ADVANCE 35 LP LOW PROFILE BALLOON CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code DQY·May 7, 2019
ADVANCE 35 LP LOW PROFILE BALLOON CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code DQY·July 14, 2017