594 results
·
48ms
·
Sources: EU EUDAMED, US FDA
CUSTOM HIPO FEMORAL BROACH
FDA Adverse Event
Malfunction
·HAYES MEDICAL INC.·Product code HTQ·September 6, 1996
CONSENSUS HIP SYSTEM
FDA Adverse Event
Malfunction
·HAYES MEDICAL, INC.·Product code KWY·February 12, 2002
CONSENSUS HIP SYSTEM / BIPOLAR SYS.
FDA Adverse Event
Other
·HAYES MEDICAL, INC.·Product code KXA·December 9, 2003
CONSENSUS KNEE SYSTEM
FDA Adverse Event
Other
·HAYES MEDICAL, INC.·Product code HSH·November 14, 2003
UNISYN HIP SYSTEM
FDA Adverse Event
Other
·HAYES MEDICAL, INC.·Product code JDI·August 13, 2003
UNISYN HIP SYSTEM
FDA Adverse Event
Other
·HAYES MEDICAL, INC.·Product code JDI·August 13, 2003
CONSENSUS HIP SYSTEM
FDA Adverse Event
Malfunction
·HAYES MEDICAL, INC.·Product code KWY·September 22, 2000
UNISYN TOTAL HIP SYSTEM
FDA Adverse Event
Injury
·HAYES MEDICAL, INC.·Product code JDI·June 6, 2007
UNISYN HIP SYSTEM
FDA Adverse Event
Other
·HAYES MEDICAL, INC.·Product code LWJ·July 14, 2004
STARTER BROACH WITH DISTAL BULLET (14MM)
FDA Adverse Event
Malfunction
·HAYES MEDICAL, INC.·Product code HTQ·May 20, 1999
CONSENSUS PRIMARY KNEE SYSTEM
FDA Adverse Event
Other
·HAYES MEDICAL, INC.·Product code JWH·October 19, 2000
UNISYN HIP SYSTEM
FDA Adverse Event
Injury
·HAYES MEDICAL, INC.·Product code JDI·August 11, 2004
UNISYN TOTAL HIP SYSTEM
FDA Adverse Event
Injury
·HAYES MEDICAL, INC.·Product code JDI·December 21, 2007
UNISYN HIP SYSTEM
FDA Adverse Event
Malfunction
·HAYES MEDICAL, INC.·Product code LWJ·April 13, 2004
PORTABLE DISTRACTION DEVICE
FDA Adverse Event
Other
·HAYES MEDICAL, INC.·Product code HST·June 8, 1998
CONSENSUS BIPOLAR HEAD, COCR, SZ.46
FDA Adverse Event
Other
·HAYES MEDICAL, INC.·Product code KWY·November 30, 1998
CONSENSUS BIPOLAR HEAD, COCR, SZ.43MM
FDA Adverse Event
Other
·HAYES MEDICAL, INC.·Product code KWY·November 25, 1998
CONSENSUS ACETABULAR SHELL, SZ.56MM
FDA Adverse Event
Other
·HAYES MEDICAL, INC.·Product code KWB·November 25, 1998
PSI FEMORAL HIP IMPLANT IMPACTOR
FDA Adverse Event
Malfunction
·HAYES MEDICAL, INC.·Product code HWA·February 3, 1999
FEMORAL ALIGNMENT GUIDE
FDA Adverse Event
Malfunction
·HAYES MEDICAL, INC.·Product code LXH·March 26, 1999