41 results · 57ms · Sources: EU EUDAMED, US FDA

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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