7 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
DIRECT LATERAL INSTRUMENTS
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code LXH·August 25, 2025
DIRECT LATERAL INSTRUMENTS
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code LXH·January 24, 2025
INTERSTIM II
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO·Product code EZW·February 4, 2013
PLMA DVC V11.51 1 R
FDA Adverse Event
Malfunction
·HOSPIRA, INC.·Product code FRN·November 9, 2010
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 5, 2014
DIRECT LATERAL INSTRUMENTS
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code LXH·October 16, 2024
DIRECT LATERAL INSTRUMENTS
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code LXH·March 4, 2025