10 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·May 12, 2024
SENSATION PLUS 8FR. 50CC IAB & ACCESSORIES (W/PRESSURE TUBES, NO STYLET)
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·December 18, 2024
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·May 15, 2024
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·May 6, 2024
TUFF IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·May 15, 2024
MECHANICAL (MANUAL) WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code IOR·March 12, 2013
X8000 LIGHTSOURCE
FDA Adverse Event
Malfunction
·STRYKER ENDOSCOPY SAN JOSE·Product code FCW·February 3, 2011
GE OEC 9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·February 21, 2008
EDWARDS LOCKING SYRINGE
FDA Adverse Event
Malfunction
·EDWARDS LIFESCIENCES·Product code MAV·June 16, 2023
EDWARDS LOCKING SYRINGE
FDA Adverse Event
Malfunction
·EDWARDS LIFESCIENCES LLC·Product code MAV·March 29, 2022