27 results
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29ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
ACUVUE OASYS CONTACT LENSES
FDA Adverse Event
Injury
·VISTAKON·Product code LPL·August 15, 2008
ACCUVUE ADVANCE
FDA Adverse Event
Injury
·VISTAKON·Product code LPL·October 19, 2007
OCTRODE LEAD KIT, 60CM LENGTH
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION (PUERTO RICO, LLC)·Product code LGW·November 13, 2022
TENDRIL ST
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code NVN·April 20, 2023
INFUSION DEVICES - UNKNOWN
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·July 31, 2024
QUATTRODE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·July 23, 2013
EON MINI
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·July 23, 2013
QUATTRODE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·July 23, 2013
ZIMMER
FDA Adverse Event
Malfunction
·ZIMMER·Product code JDI·January 24, 2005
BAXTER
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORP.·Product code FPA·April 7, 1999
STERI-OSS DENTAL IMPLANT
FDA Adverse Event
Malfunction
·STERI-OSS, INC.·Product code DZE·September 2, 1997
CAPD SOLUTION TRANSFER SET (SHORT) FOR UV-FLASH
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORP.·Product code KDJ·February 23, 2001
ACCENT DR RF PACEMAKER
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code NVZ·May 24, 2021
RESPIRONICS
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code MNT·February 7, 2023
UNK - PLATES: LOCKING: CALCANEAL PLATE
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code HRS·May 19, 2021
UNK - SCREWS: LOCKING: CALCANEAL
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code HWC·May 19, 2021
CNS-9700A
FDA Adverse Event
Malfunction
·NIHON KOHDEN CORPORATION·Product code MHX·April 2, 2020
CNS-6201A
FDA Adverse Event
Malfunction
·NIHON KOHDEN CORPORATION·Product code MHX·August 22, 2018
ZM-520PA
FDA Adverse Event
Malfunction
·NIHON KOHDEN CORPORATION·Product code DRT·August 21, 2018
NI
FDA Adverse Event
Malfunction
·NIHON KOHDEN CORPORATION·Product code MHX·January 7, 2020