234 results · 20ms · Sources: EU EUDAMED, US FDA

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MONOPOLAR CABLE, ELECTROSURGICAL ACCESSORIES

FDA Adverse Event
Malfunction ·BOWA ELECTRONIC ZUBEHOR FUR ELEKTROCHIRU·Product code FFZ·March 19, 2004

UNIVERSAL ACTIVE CORD

FDA Adverse Event
Injury ·WILSON-COOK MEDICAL, INC.·Product code FFZ·January 12, 2004

A CORD

FDA Adverse Event
Malfunction ·OLYMPUS MEDICAL SYSTEMS CORPORATION·Product code FFZ·June 13, 2014

OLYMPUS ACTIVE CORD

FDA Adverse Event
Malfunction ·OLYMPUS MEDICAL SYSTEM CORPORATION·Product code FFZ·April 6, 2012

DISPOSABLE ACTIVE CORD

FDA Adverse Event
Malfunction ·CIRCON ACMI·Product code FFZ·March 11, 2002

*

FDA Adverse Event
Malfunction ·KARL STORZ ENDOSCOPY-AMERICA, INC.·Product code FFZ·October 10, 2003

UNIVERSAL ACTIVE CORD

FDA Adverse Event
Malfunction ·WILSON-COOK MEDICAL, INC.·Product code FFZ·October 27, 2003

OLYMPUS

FDA Adverse Event
Malfunction ·OLYMPUS OPTICAL CO. LTD·Product code FFZ·December 29, 2003

OLYMPUS

FDA Adverse Event
Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code FFZ·July 11, 2003

*

FDA Adverse Event
Injury ·ASPEN SURGICAL PRODUCTS, INC·Product code FFZ·August 20, 2003

USA ELITE/USA SERIES DISPOSABLE ACTIVE CORD

FDA Adverse Event
Malfunction ·CIRCON ACMI·Product code FFZ·June 19, 2000

USA ELITE/USA SERIES DISPOSABLE ACTIVE CORD

FDA Adverse Event
Malfunction ·CIRCON ACMI·Product code FFZ·April 18, 2000

CIRCON ACMI

FDA Adverse Event
Malfunction ·CIRCON ACMI·Product code FFZ·April 18, 2000

UNIVERSAL ACTIVE CORD

FDA Adverse Event
Malfunction ·WILSON-COOK MEDICAL, INC.·Product code FFZ·June 3, 2005

*

FDA Adverse Event
Malfunction ·SRI/SURGICAL EXPRESS, INC.·Product code FFZ·April 11, 2005

DISPOSABLE ACTIVE CORD

FDA Adverse Event
Malfunction ·CIRCON ACMI·Product code FFZ·August 26, 1997

*

FDA Adverse Event
Malfunction ·KARL STORZ ENDOSCOPY-AMERICA, INC.·Product code FFZ·July 16, 1997

DAC DISPOSABLE ACTIVE CORD

FDA Adverse Event
Other ·CIRCON ACMI·Product code FFZ·August 15, 1997

*

FDA Adverse Event
Injury ·*·Product code FFZ·January 17, 2007

1221826-2007-00001

FDA Adverse Event
Other ·Product code FFZ·January 11, 2007