27 results · 29ms · Sources: EU EUDAMED, US FDA

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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