9 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
PROCEED MESH
FDA Adverse Event
Injury
·ETHICON INC.·Product code FTL·September 25, 2018
OCTRODE LEAD KIT, 60CM LENGTH
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION (PUERTO RICO, LLC)·Product code LGW·March 4, 2025
OCTRODE LEAD KIT, 60CM LENGTH
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION (PUERTO RICO, LLC)·Product code LGW·March 5, 2025
SWIFT-LOCK ANCHOR
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code GZB·March 5, 2025
ORION RC SCS IPG
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code LGW·March 5, 2025
DUR DYNAMIC LOCK RING 60 OR 72
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS·Product code LPH·May 14, 2013
VALIANT
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·September 23, 2014
UNICEL® DXC 800 PRO SYNCHRON® CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·June 1, 2011
PREVENA PLUS¿ INCISION MANAGEMENT SYSTEM
FDA Adverse Event
Injury
·KINETIC CONCEPTS, INC.·Product code OMP·July 19, 2019