8 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
PUMP, INFUSION, IMPLANTED, PROGRAMMABLE
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code LKK·May 8, 2013
DADE INNOVIN
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GJS·September 18, 2014
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·May 23, 2011
SYNCHROMED II
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·September 2, 2015
OXFORD UNI KNEE PHASE III 4.0MM DIAM. FEMORAL DRILL
FDA Adverse Event
Malfunction
·BIOMET ORTHOPEDICS·Product code HTW·November 20, 2009
SYNCHROMED II
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·September 2, 2015
OXFORD MP 04MM DRILL
FDA Adverse Event
Malfunction
·BIOMET ORTHOPEDICS·Product code NRA·April 13, 2017
OXFORD PH3 CEMENTLESS FEM SZ M
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code NRA·June 20, 2025