6 results
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21ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
RIATA ACTIVE FIXATION
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·May 8, 2014
UNKNOWN LEFT REJUVENATE/ABGII HIP
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS MAHWAH·Product code MEH·October 17, 2012
CAROTID WALLSTENT MONORAIL
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - GALWAY·Product code NIM·August 16, 2010
INTELLIS
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·April 10, 2018
1.5 LACTOSORB SYSTEM 1.5 X 4 MM LACTOSORB SCREW
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code NHB·March 20, 2018
1.5 LACTOSORB SYSTEM 1.5 X 4 MM LACTOSORB SCREW
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code NHB·March 20, 2018