53 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
6000030-1997-00238
FDA Adverse Event
Malfunction
·MEDTRONIC INC·Product code LKK·August 29, 1997
6000030-2006-00073
FDA Adverse Event
Malfunction
·RICE CREEK MFG·Product code LKK·January 13, 2006
PUMP, INFUSION, IMPLANTED, PROGRAMMABLE
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code LKK·January 19, 2018
MEDTRONIC
FDA Adverse Event
Malfunction
·MEDTRONIC INC. USA·Product code LKK·October 25, 2004
INDURA
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code LKK·August 24, 2007
INDURA
FDA Adverse Event
Malfunction
·RICE CREEK MANUFACTURING·Product code LKK·September 27, 2007
SYNCHROMED II
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·February 9, 2009
DURAMAX CHRONIC HEMODIALYSIS CATHETER
FDA Adverse Event
Malfunction
·ANGIODYNAMICS·Product code MSD·February 18, 2011
SYNCHROMED II
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code LKK·July 3, 2013
INDURA CATHETER
FDA Adverse Event
Malfunction
·RICE CREEK MANUFACTURING·Product code LKK·December 28, 2006
SYNCHROMED EL
FDA Adverse Event
Malfunction
·RICE CREEK MANUFACTURING·Product code LKK·December 28, 2006
INDURA
FDA Adverse Event
Malfunction
·RICE CREEK MANUFACTURING·Product code LKK·December 21, 2006
SYNCHROMED II
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·July 30, 2010
SYNCHROMED II
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code LKK·October 12, 2010
SYNCHROMED II
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code LKK·July 14, 2009
SYNCHROMED II
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·May 16, 2013
SYNCHROMED EL
FDA Adverse Event
Malfunction
·RICE CREEK MFG·Product code LKK·January 7, 2015
INTELLIS
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·December 6, 2019
INDURA
FDA Adverse Event
Malfunction
·RICE CREEK MANUFACTURING·Product code LKK·June 5, 2007
SYNCHROMED EL
FDA Adverse Event
Malfunction
·RICE CREEK MANUFACTURING·Product code LKK·June 5, 2007