10 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
TSRH SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·October 27, 2011
TSRH SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·October 27, 2011
TSRH SPINAL SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code KWP·February 18, 2011
TSRH SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPAEDIC INC.·Product code KWP·October 8, 2009
TSRH SPINAL SYSTEM
FDA Adverse Event
WARSAW ORTHOPEDIC, INC.·Product code KWP·May 20, 2011
TSRH SPINAL SYSTEM
FDA Adverse Event
WARSAW ORTHOPEDIC, INC.·Product code KWP·May 20, 2011
TSRH SPINAL SYSTEM
FDA Adverse Event
WARSAW ORTHOPEDIC, INC.·Product code KWP·May 20, 2011
APEX HOLE ELIM POSITIVE STOP
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.-1818910·Product code LPH·June 25, 2014
CE INFUSOR SV 2, 12 PACK
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code MEB·November 9, 2010
PLUM XL PUMP
FDA Adverse Event
Malfunction
·HOSPIRA, INC.·Product code FRN·November 25, 2008