10,000 results · 73ms · Sources: EU EUDAMED, US FDA

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QUICKIE QRI

FDA Adverse Event
Malfunction ·SUNRISE MEDICAL PRIVADA MISIONES·Product code IOR·October 5, 2017

QUICKIE QRI

FDA Adverse Event
Malfunction ·SUNRISE MEDICAL PRIVADA MISIONES·Product code IOR·December 20, 2013

QUICKVUE AT-HOME OTC COVID-19 TEST

FDA Adverse Event
Malfunction ·QUIDEL CORPORATION·Product code QKP·August 17, 2021

WALGREENS COVID-19 & FLU A + B ANTIGEN TEST

FDA Adverse Event
Malfunction ·HEALGEN SCIENTIFIC LLC·Product code SCA·August 12, 2025

X-GUIDE SURGICAL NAVIGATION SYSTEM

FDA Adverse Event
Malfunction ·X-NAV TECHNOLOGIES, LLC·Product code QRY·November 13, 2024

BD RAPID DETECTION OF SARS-COV-2 VERITOR

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code QKP·April 26, 2021

BD RAPID DETECTION OF SARS-COV-2 VERITOR

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code QKP·April 26, 2021

BD RAPID DETECTION OF SARS-COV-2 VERITOR¿

FDA Adverse Event
Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code QKP·January 18, 2022

BD RAPID DETECTION OF SARS-COV-2 VERITOR¿

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code QKP·January 18, 2022

SFX SPI PDS+ UNI VIO 12IN 0 S/A CT-1

FDA Adverse Event
Malfunction ·ETHICON INC.·Product code NEW·September 13, 2022

SFX SPI PDS+ UNI VIO 12IN 0 S/A CT-1

FDA Adverse Event
Malfunction ·ETHICON INC.·Product code NEW·September 13, 2022

BD ALARIS PUMP MODULE SMARTSITE INFUSION SET

FDA Adverse Event
Malfunction ·SISTEMAS MEDICOS ALARIS S.A DE C.V.·Product code FPA·May 14, 2026

BD ALARIS SMARTSITE LOW SORBING SECONDARY SET

FDA Adverse Event
Malfunction ·SISTEMAS MEDICOS ALARIS S.A DE C.V.·Product code FPA·May 22, 2026

COVID-19 TEST KIT

FDA Adverse Event
Malfunction ·LUMINEX ARIES·Product code QJR·July 24, 2020

COVID-19 TEST KIT

FDA Adverse Event
Malfunction ·LUMINEX ARIES·Product code QJR·July 24, 2020

MEDALLION STERILIZER

FDA Adverse Event
Malfunction ·STERIS CORPORATION - ERIE·Product code FLE·March 19, 2004

16" EAGLE 2000 GRAVITY STERILIZER

FDA Adverse Event
Malfunction ·STERIS CORPORATION - ERIE·Product code FLE·October 10, 2003

OXYGEN REGULATOR

FDA Adverse Event
Malfunction ·ERIE MFG. CO.·Product code CAX·February 11, 1994

BOND PLUS SLIDES

FDA Adverse Event
Malfunction ·ERIE SCIENTIFIC COMPANY·Product code KEW·October 22, 2025

EAGLE TEN STERILIZER

FDA Adverse Event
Malfunction ·STERIS CORPORATION - ERIE·Product code FLE·January 7, 2005