10 results
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25ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
THERMOCOOL® SF NAV UNI-DIRECTIONAL CATHETER
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code LPB·May 20, 2014
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·November 6, 2012
ECHELON*FLEX60 LONG
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·August 31, 2010
UNKNOWN ENDO GIA SULU
FDA Adverse Event
Injury
·UNITED STATES SURGICAL·Product code GDW·March 12, 2010
UNKNOWN ENDO GIA SULU
FDA Adverse Event
Injury
·UNITED STATES SURGICAL·Product code GDW·March 12, 2010
UNKNOWN ENDO GIA SULU
FDA Adverse Event
Injury
·UNITES STATES SURGICAL·Product code GDW·March 12, 2010
UNKNOWN ENDO GIA SULU
FDA Adverse Event
Injury
·UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHCARE GROUP·Product code GDW·March 12, 2010
UNKNOWN ENDO GIA SULU
FDA Adverse Event
Injury
·UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHCARE GROUP·Product code GDW·March 12, 2010
UNK - IMPLANT
FDA Adverse Event
Injury
·DEPUY MITEK LLC US·Product code HWC·November 30, 2021
UNKNOWN ENDO GIA SULU
FDA Adverse Event
Injury
·UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHCARE GROUP·Product code GDW·March 12, 2010