594 results · 48ms · Sources: EU EUDAMED, US FDA

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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