14 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
INNOVA 4100
FDA Adverse Event
Malfunction
·GE MEDICAL SYSTEMS·Product code MQB·April 4, 2011
INNOVA 4100
FDA Adverse Event
Malfunction
·GE MEDICAL SYSTEMS·Product code MQB·May 6, 2011
FOLYSIL SILICONE CATHETER
FDA Adverse Event
Malfunction
·COLOPLAST A/S·Product code EZL·August 28, 2024
RADIESSE INJECTABLE IMPLANT
FDA Adverse Event
Injury
·MERZ NORTH AMERICA, INC·Product code LMH·July 24, 2024
FOLYSIL SILICONE CATHETER
FDA Adverse Event
Malfunction
·COLOPLAST A/S·Product code EZL·August 28, 2024
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·March 27, 2013
LMA UNIQUE
FDA Adverse Event
Malfunction
·THE LARYNGEAL MASK COMPANY LIMITED·Product code CAE·March 16, 2011
LIFEPAK 20 DEFIBRILLATOR/MONITOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC.·Product code LDD·March 26, 2008
PROTEGO PROMRI S 65
FDA Adverse Event
Malfunction
·BIOTRONIK SE & CO. KG·Product code NVY·November 18, 2024
FOLYSIL SILICONE CATHETER
FDA Adverse Event
Malfunction
·COLOPLAST A/S·Product code EZL·August 23, 2024
FOLYSIL SILICONE CATHETER
FDA Adverse Event
Malfunction
·COLOPLAST A/S·Product code EZL·September 19, 2024
FOLYSIL SILICONE CATHETER
FDA Adverse Event
Malfunction
·COLOPLAST A/S·Product code EZL·August 27, 2024
SMR REVERSE HUMERAL BODY
FDA Adverse Event
Injury
·LIMACORPORATE S.P.A·Product code PHX·May 12, 2023
FOLYSIL SILICONE CATHETER
FDA Adverse Event
Malfunction
·COLOPLAST A/S·Product code EZL·December 19, 2024