10,000 results
·
73ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
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