377 results
·
47ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Death
×
LAG SCREW INSERTER
FDA Adverse Event
Death
·ZIMMER PRODUCT SERVICE·Product code HXX·August 11, 1994
IMPLANT TAPERED 9X11X25MM
FDA Adverse Event
Death
·THEKEN SPINE·Product code MQP·December 3, 2010
BRAT
FDA Adverse Event
Death
·COBE CARDIOVASCULAR INC. DIV SORIN BIOMEDICAL INC·Product code CAC·February 8, 2001
DE PUY
FDA Adverse Event
Death
·*·Product code LXH·May 31, 2005
COATED VICRYL (POLYGLACTIN 910) SUTURE
FDA Adverse Event
Death
·ETHICON, INC. SAN ANGELO·Product code GAM·October 12, 1999
CRS® ROTARY MIXER CEMENT 5CC STERILE
FDA Adverse Event
Death
·SYNTHES MONUMENT·Product code GXP·January 24, 2014
HANA ORTHOPEDIC SURGERY TABLE
FDA Adverse Event
Death
·MIZUHO OSI·Product code JEA·December 5, 2018
ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
FDA Adverse Event
Death
·NUVASIVE INC.·Product code LXH·May 29, 2020
MANUAL ORTHOPEDIC SURGICAL INSTRUMENT
FDA Adverse Event
Death
·MEDTRONIC SOFAMOR DANEK·Product code FZX·September 13, 2012
ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
FDA Adverse Event
Death
·NUVASIVE·Product code LXH·October 10, 2019
SURGICAL SIMPLEX P
FDA Adverse Event
Death
·HOWMEDICA INC·Product code LOD·September 26, 1997
BONE CEMENT
FDA Adverse Event
Death
·ZIMMER·Product code LOD·May 7, 1997
ARTOSCAN
FDA Adverse Event
Death
·ESAOTE S.P.A.·Product code LNH·December 22, 2000
COBE BRAT 2 AUTOLOGOUS TRANSFUSION SYSTEM
FDA Adverse Event
Death
·COBE CARDIOVASCULAR, INC.·Product code CAC·April 21, 1999
ARTOSCAN
FDA Adverse Event
Death
·ESAOTE S.P.A.·Product code LNH·May 25, 2001
UNK
FDA Adverse Event
Death
·*·Product code JEA·September 22, 2006
DD+ MECHANICAL QUAL DEVICE
FDA Adverse Event
Death
·ST. JUDE MEDICAL, INC.(CRM-SUNNYVALE)·Product code LWS·November 29, 2016
NUVASIVE POLYAXIAL SPINAL SCREWS
FDA Adverse Event
Death
·NUVASIVE, INC.·Product code NKB·August 18, 2017
AUTOVAC POST-OPERATIVE ORTHOPEDIC AUTOTRANSFUSION SYSTEM
FDA Adverse Event
Death
·BOEHRINGER LABORATORIES, INC.·Product code CAC·June 20, 1994
OPTIPAC 40 REFOBACIN BONE CEMENT R-3
FDA Adverse Event
Death
·BIOMET FRANCE S.A.R.L.·Product code MBB·May 10, 2019