10,000 results
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83ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PINNACLE ULTAMET METAL INSERT
FDA Adverse Event
Malfunction
·DEPUY ORTHOPAEDICS·Product code KWA·July 8, 2013
C-TAPER LFIT ANATOMIC HEAD
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS·Product code KWY·July 8, 2013
STRYKER TRIATHLON KNEE SYSTEM
FDA Adverse Event
Malfunction
·STRYKER ORTHOPEDICS·Product code JWH·April 12, 2013
TRILOGY 100
FDA Adverse Event
Malfunction
·RESPIRONICS INC.·Product code CBK·February 1, 2022
TRILOGY 202
FDA Adverse Event
Malfunction
·RESPIRONICS INC.·Product code CBK·February 2, 2022
AVEA VENTILATOR
FDA Adverse Event
Injury
·VYAIRE MEDICAL, INC·Product code CBK·December 13, 2017
AVEA VENTILATOR
FDA Adverse Event
Malfunction
·VYAIRE MEDICAL·Product code CBK·November 2, 2018
AVEA VENTILATOR
FDA Adverse Event
Malfunction
·VYAIRE MEDICAL, INC·Product code CBK·December 21, 2017
COBALT CHROME TAPER FEMORAL HEAD
FDA Adverse Event
SMITH AND NEPHEW·Product code LZO·May 6, 2013
PRESSFT
FDA Adverse Event
Malfunction
·LINVATEC CORPORATION D/B/A CONMED LINVATEC·Product code MAI·July 24, 2013
AVEA VENTILATOR
FDA Adverse Event
Malfunction
·VYAIRE MEDICAL, INC·Product code CBK·November 28, 2017
AVEA VENTILATOR
FDA Adverse Event
Malfunction
·VYAIRE MEDICAL·Product code CBK·February 13, 2019
SONOPET DISPOSABLE TUBING SET AND EXTENDER FILTER TUBING
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS,DIV OF STRYKER CORP·Product code LFL·July 29, 2013
AVEA VENTILATOR
FDA Adverse Event
Malfunction
·VYAIRE MEDICAL, INC·Product code CBK·June 20, 2018
VELA VENTILATOR
FDA Adverse Event
Injury
·CAREFUSION, INC·Product code CBK·December 2, 2016
VELA VENTILATOR
FDA Adverse Event
Malfunction
·VYAIRE MEDICAL·Product code CBK·July 26, 2019
AVEA VENTILATOR
FDA Adverse Event
Malfunction
·VYAIRE MEDICAL, INC·Product code CBK·October 27, 2017
VELA VENTILATOR
FDA Adverse Event
Malfunction
·VYAIRE MEDICAL, INC·Product code CBK·November 22, 2017
ALTRUA
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·July 14, 2011
ACCOLADE
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWP·October 9, 2017