41 results
·
57ms
·
Sources: EU EUDAMED, US FDA
EPS PLICATOR INSTRUMENT
FDA Adverse Event
Injury
·NDO SURGICAL, INC.·Product code KOG·May 16, 2007
PLICATOR
FDA Adverse Event
Injury
·NDO SURGICAL, INC.·Product code KOG·November 30, 2007
PLICATOR
FDA Adverse Event
Injury
·NDO SURGICAL, INC.·Product code KOG·April 29, 2005
PLICATOR
FDA Adverse Event
Injury
·NDO SURGICAL, INC.·Product code KOG·February 12, 2007
PLICATOR
FDA Adverse Event
Malfunction
·NDO SURGICAL, INC.·Product code KOG·March 9, 2007
PLICATOR
FDA Adverse Event
Injury
·NDO SURGICAL, INC.·Product code KOG·January 3, 2007
PLICATOR
FDA Adverse Event
Injury
·NDO SURGICAL, INC.·Product code KOG·January 7, 2006
PLICATOR
FDA Adverse Event
Injury
·NDO SURGICAL, INC.·Product code ODE·January 7, 2006
PLICATOR
FDA Adverse Event
Injury
·NDO SURGICAL, INC.·Product code KOG·December 30, 2006
PLICATOR
FDA Adverse Event
Injury
·NDO SURGICAL, INC.·Product code KOG·December 30, 2006
PLICATOR
FDA Adverse Event
Injury
·NDO SURGICAL, INC.·Product code KOG·December 4, 2007
PLICATOR
FDA Adverse Event
Injury
·NDO SURGICAL, INC.·Product code KOG·February 18, 2005
EPS/PLICATOR
FDA Adverse Event
Injury
·NDO SURGICAL, INC.·Product code KOG·June 14, 2007
PLICATOR
FDA Adverse Event
Death
·NDO SURGICAL, INC·Product code KOG·August 29, 2005
PLICATOR
FDA Adverse Event
Injury
·NDO SURGICAL, INC.·Product code KOG·July 1, 2005
Plicator EPS Plication System Catalog Number: 160-01128R
FDA Recall
Terminated
·NDO Surgical, Inc.·Product code KOG·January 26, 2007
ENDOPATH
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGICAL, INC.·Product code GDW·December 22, 2009
HARMONIC ACE SHEARS, ERG HANDLE, CURVED BLADE
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGICAL, INC.·Product code NLQ·April 18, 2013
ETHICON TVP
FDA Adverse Event
Injury
·ETHICON ENDO-SURGICAL, INC.·Product code GAG·April 1, 1997
ENDOPATH DISPOSABLE SURGICAL TROCAR
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGICAL, INC.·Product code GCJ·October 15, 1996