155 results
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39ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Injury
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ACCU-CHEK ULTRAFLEX INFUSION SET
FDA Adverse Event
Injury
·ROCHE INSULIN DELIVERY SYSTEMS, INC.·Product code FPA·January 12, 2012
ACCU-CHEK SPIRIT
FDA Adverse Event
Injury
·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code LZG·January 12, 2012
BIOROOT RCS
FDA Adverse Event
Injury
·SEPTODONT, INC.·Product code KIF·October 23, 2017
BIOROOT RCS
FDA Adverse Event
Injury
·SEPTODONT SAS·Product code KIF·August 28, 2023
BIOROOT RCS
FDA Adverse Event
Injury
·SEPTODONT, INC.·Product code KIF·July 4, 2017
PATIENT INFORMATION CENTER IX
FDA Adverse Event
Injury
·PHILIPS NORTH AMERICA LLC·Product code MHX·June 6, 2022
NV MICROCATHETER
FDA Adverse Event
Injury
·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·November 10, 2023
CAIRE STROLLER PORTABLE
FDA Adverse Event
Injury
·CAIRE, INC.·Product code BYJ·April 13, 2010
PATIENT INFORMATION CENTER IX
FDA Adverse Event
Injury
·PHILIPS NORTH AMERICA LLC·Product code MHX·December 27, 2021
OLYMPUS RC+S
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·July 20, 2021
SUMMIT RC+S
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·October 1, 2024
NUCLEUS 24 RCS
FDA Adverse Event
Injury
·COCHLEAR LTD.·Product code MCM·May 7, 2004
NUCLEUS CI24 RCS
FDA Adverse Event
Injury
·COCHLEAR LTD·Product code MCM·May 7, 2004
SUMMIT RC+S
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·October 17, 2023
THERMOCOOL® SF NAV UNI-DIRECTIONAL CATHETER
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code LPB·August 29, 2024
COAGUCHECK XS
FDA Adverse Event
Injury
·ROCHE DIAGNOSTICS GMBH·Product code GJS·December 4, 2024
COAGUCHECK XS
FDA Adverse Event
Injury
·ROCHE DIAGNOSTICS GMBH·Product code GJS·December 4, 2024
COAGUCHECK XS
FDA Adverse Event
Injury
·ROCHE DIAGNOSTICS GMBH·Product code GJS·December 4, 2024
PATIENT INFORMATION CENTER IX
FDA Adverse Event
Injury
·PHILIPS MEDICAL SYSTEMS·Product code MHX·August 8, 2023
ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM
FDA Adverse Event
Injury
·CORDIS NEUROVASCULAR, INC.·Product code NJE·November 1, 2011