101 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Injury
×
EXPANSE BLOOD BANK
FDA Adverse Event
Injury
·MEDICAL INFORMATION TECHNOLOGY, INC.·Product code MMH·December 18, 2025
FEMORAL LOCKING NAIL SMALL DIA., LEFT D11X400 MM
FDA Adverse Event
Injury
·STRYKER TRAUMA KIEL·Product code HSB·April 13, 2005
BAK/CERVICAL (BAK/C)
FDA Adverse Event
Injury
·SULZER SPINE TECH·Product code MAX·July 21, 2003
BAK/CERVICAL (BAK/C)
FDA Adverse Event
Injury
·SULZER SPINE TECH·Product code MAX·June 4, 2003
BAK/PROXIMITY
FDA Adverse Event
Injury
·CENTERPULSE SPINE-TECH (SULZER-SPINETECH)·Product code MAX·March 7, 2003
BAK INSTRUMENTATION
FDA Adverse Event
Injury
·SULZER SPINE-TECH·Product code LXH·August 3, 1998
BAK INSTRUMENTATION
FDA Adverse Event
Injury
·SULZER SPINE-TECH·Product code LXH·August 13, 1998
BAK CAGE
FDA Adverse Event
Injury
·ZIMMER CORP.·Product code MAX·September 14, 2004
BAK/CAGE
FDA Adverse Event
Injury
·SULZER SPINE-TECH·Product code MAX·July 17, 2002
BAK INSTRUMENT
FDA Adverse Event
Injury
·SULZER SPINE-TECH·Product code HTO·February 24, 2000
BAK/C
FDA Adverse Event
Injury
·SULZER SPINE-TECH·Product code MAX·June 3, 2003
BAK/VISTA
FDA Adverse Event
Injury
·ZIMMER SPINE, INC.·Product code MAX·September 3, 2009
BAK CAGES
FDA Adverse Event
Injury
·ALLIED ORTHOPEDIC ASSOC.·Product code MAX·January 9, 1998
BAK INSTRUMENTATION
FDA Adverse Event
Injury
·SULZER SPINE-TECH·Product code LXH·June 15, 1998
BAK LUMBAR CAGE
FDA Adverse Event
Injury
·SPINE-TECH·Product code MAX·November 12, 2003
BAK IMPLANT GENERIC
FDA Adverse Event
Injury
·ZIMMER SPINE·Product code MAX·July 27, 2015
BAK TITANIUM CAGE
FDA Adverse Event
Injury
·SPINE TECH·Product code MAX·August 4, 2000
BAK TITANIUM CAGE
FDA Adverse Event
Injury
·Product code MAX·March 26, 2014
BAK INTERBODY FUSION
FDA Adverse Event
Injury
·SPINE-TECH·Product code MAX·December 3, 2000
BAK/L GENERIC
FDA Adverse Event
Injury
·ZIMMER SPINE·Product code MAX·May 14, 2013