94 results · 488ms · Sources: EU EUDAMED, US FDA

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TOSHIBA

FDA Adverse Event
Death ·TOSHIBA MEDICAL SYSTEMS CORPORATION·Product code ITX·November 13, 2008

TOSHIBA

FDA Adverse Event
Malfunction ·TOSHIBA MEDICAL SYSTEMS CORPORATION·Product code ITX·September 16, 2015

TOSHIBA

FDA Adverse Event
Injury ·TOSHIBA MEDICAL SYSTEMS CORPORATION·Product code JAK·February 3, 2012

TOSHIBA

FDA Adverse Event
Injury ·TOSHIBA MEDICAL SYSTEMS CORPORATION·Product code MQB·June 24, 2014

TOSHIBA

FDA Adverse Event
Injury ·TOSHIBA MEDICAL SYSTEMS CORPORATION·Product code MOS·June 11, 2014

TOSHIBA

FDA Adverse Event
Other ·TOSHIBA MEDICAL SYSTEMS CORPORATION·Product code MOS·April 12, 2010

TOSHIBA

FDA Adverse Event
Injury ·TOSHIBA MEDICAL SYSTEMS CORPORATION·Product code LNH·June 9, 2010

TOSHIBA

FDA Adverse Event
Other ·TOSHIBA MEDICAL SYSTEMS CORPORATION·Product code KXJ·April 1, 2010

TOSHIBA

FDA Adverse Event
Malfunction ·TOSHIBA MEDICAL SYSTEMS CORPORATION·Product code JAK·February 2, 2004

TOSHIBA

FDA Adverse Event
Other ·TOSHIBA MEDICAL SYSTEMS CORPORATION·Product code LNH·March 2, 2004

TOSHIBA

FDA Adverse Event
Other ·TOSHIBA MEDICAL SYSTEMS CORPORATION·Product code LNH·March 2, 2004

TOSHIBA

FDA Adverse Event
Malfunction ·TOSHIBA MEDICAL SYSTEMS CORPORATION·Product code ITX·December 4, 2012

TOSHIBA

FDA Adverse Event
Injury ·TOSHIBA MEDICAL SYSTEMS CORPORATION·Product code LNH·October 17, 2014

APLIO XG

FDA Adverse Event
Malfunction ·TOSHIBA MEDICAL SYSTEMS CORPORATION·Product code ITX·November 9, 2017

X08A

FDA Adverse Event
Malfunction ·TOSHIBA MEDICAL SYSTEMS CORPORATION·Product code LNH·November 9, 2017

TITAN

FDA Adverse Event
Malfunction ·TOSHIBA MEDICAL SYSTEMS CORPORATION·Product code LNH·November 8, 2017

TOSHIBA

FDA Adverse Event
Injury ·TOSHIBA MEDICAL SYSTEMS CORPORATION·Product code JAK·June 21, 2012

TOSHIBA

FDA Adverse Event
Injury ·TOSHIBA MEDICAL SYSTEMS CORPORATION·Product code JAK·May 10, 2012

TOSHIBA

FDA Adverse Event
Injury ·TOSHIBA MEDICAL SYSTEMS CORPORATION·Product code JAK·April 27, 2012

TOSHIBA

FDA Adverse Event
Injury ·TOSHIBA MEDICAL SYSTEMS CORPORATION·Product code JAK·March 9, 2012