62 results
·
93ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
TRICON/GENESIS KNEE
FDA Adverse Event
Injury
·SMITH & NEPHEW INC. ORTHOPAEDICS DIV.·Product code HSH·October 30, 1997
MOD II UNICOMPARTMENTAL KNEE SYSTEM
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC., ORTHOPAEDICS DIV.·Product code HTG·September 25, 1998
MAXIM PRIMARY TIB. BEAR
FDA Adverse Event
Injury
·BIOMET, INC.·Product code HSH·January 8, 2001
SWEET TIP BIPOLAR LEAD
FDA Adverse Event
Malfunction
·CARDIAC PACEMAKERS·Product code DXY·September 8, 1997
BIOMET
FDA Adverse Event
Injury
·BIOMET, INC.·Product code JDI·January 2, 1998
VENTAK P2
FDA Adverse Event
Malfunction
·CARDIAC PACEMAKERS·Product code LWS·August 5, 1998
VENTAK AV
FDA Adverse Event
Injury
·CARDIAC PACEMAKERS·Product code LWS·February 8, 1998
ENDOTAK DOWN-SIZED PLUS
FDA Adverse Event
Injury
·CARDIAC PACEMAKERS·Product code LWS·November 7, 1997
VENTAK AV AUTOMATIC CARDIOVERTOR DEFIBRILLATOR
FDA Adverse Event
Injury
·CARDIAC PACEMAKERS·Product code LWS·November 7, 1997
SOFTFORM FACIAL IMPLANT
FDA Adverse Event
Injury
·TISSUE TECHNOLOGIES, INC.·Product code FTL·June 22, 1998
SKLAR INSTRUMENTS
FDA Adverse Event
Injury
·SKLAR INSTRUMENTS·Product code HDF·September 17, 1997
ABBOTT AXSYM SYSTEM
FDA Adverse Event
Other
·ABBOTT MANUFACTURING, INC.·Product code JJE·August 11, 1997
COATED VICRYL (POLYGLACTIN 910) SUTURE
FDA Adverse Event
Injury
·ETHICON, INC.·Product code GAM·July 13, 2004
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·June 27, 2017
NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·COCHLEAR LTD.·Product code MCM·August 14, 1997
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code KWP·May 23, 2014
DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·April 8, 2024
SHILEY CUFFLESS TRACHEOSTOMY TUBE
FDA Adverse Event
Malfunction
·MALLINCKRODT MEDICAL, INC.·Product code BTO·January 26, 1998
7200 SERIES MICROPROCESSOR VENTILAT
FDA Adverse Event
Injury
·PURITAN BENNETT·Product code CBK·November 24, 1997
ANGIO-SEAL
FDA Adverse Event
Injury
·QUINTON INSTRUMENT CO.·Product code MGB·October 7, 1997