37 results · 58ms · Sources: EU EUDAMED, US FDA

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SLIDEPREP PLUS CYTOLOGY CENTRIFUGE

FDA Adverse Event
Malfunction ·SEPARATION TECHNOLOGY, INC.·Product code JQC·December 19, 2012

SLIDEPREP PLUS CYTOLOGY CENTRIFUGE

FDA Adverse Event
Malfunction ·SEPARATION TECHNOLOGY, INC. PART OF THERMO FISHER SCIENTIFIC·Product code IFB·August 16, 2012

CLEAR-CRIT PLASTIC CAPILLARY TUBES

FDA Adverse Event
Malfunction ·SEPARATION TECHNOLOGY, INC.·Product code GIO·October 28, 1999

STAT-60

FDA Adverse Event
Malfunction ·SEPARATION TECHNOLOGY, INC.·Product code JQC·November 8, 2002

VANISHPOINT

FDA Adverse Event
Malfunction ·RETRACTABLE TECHNOLOGIES, INC.·Product code MEG·December 11, 2015

8.5F SHEATH WITH CURVE VIZ MDC

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code LPB·April 8, 2019

SLIDEPREP PLUS CYTOLOGY CENTRIFUGE

FDA Adverse Event
Malfunction ·SEPARATION TECHNOLOGY, INC., PART OF THERMO FISHER SCIENTIFIC·Product code JQC·May 1, 2013

SLIDEPREP PLUS CYTOLOGY CENTRIFUGE

FDA Adverse Event
Malfunction ·SEPARATION TECHNOLOGY, INC., PART OF THERMO FISHER SCIENTIFIC·Product code JQC·August 30, 2012

PREMILENE NON-CARDIOVASCULAR

FDA Adverse Event
Malfunction ·B.BRAUN SURGICAL SA·Product code GAW·February 19, 2018

AUTOLITH TCH 1.9FR PROBE, 375CM DS BSC

FDA Adverse Event
Malfunction ·NORTHGATE TECHNOLOGIES, INC·Product code FFK·June 29, 2022

AUTOLITH TCH 1.9FR PROBE, 375CM DS BSC

FDA Adverse Event
Malfunction ·NORTHGATE TECHNOLOGIES, INC·Product code FFK·June 29, 2022

CARTO VIZIGO¿ 8.5F BI-DIRECTIONAL GUIDING SHEATH ¿ MEDIUM

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code DYB·April 4, 2019

CARTO VIZIGO¿ 8.5F BI-DIRECTIONAL GUIDING SHEATH -

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code DYB·April 16, 2019

INTELISWAB COVID-19 RAPID TEST

FDA Adverse Event
Malfunction ·ORASURE TECHNOLOGIES INC.·Product code QKP·January 6, 2022

AUTOLITH TCH 1.9FR PROBE, 375CM DS BSC

FDA Adverse Event
Malfunction ·NORTHGATE TECHNOLOGIES, INC·Product code FFK·June 29, 2022

WEBSTER CS CATHETER WITH AUTO ID TECHNOLOGY

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code DRF·May 9, 2025

INTELISWAB COVID-19 RAPID TEST

FDA Adverse Event
Malfunction ·ORASURE TECHNOLOGIES, INC.·Product code QKP·November 29, 2023

INTELISWAB COVID-19 RAPID TEST

FDA Adverse Event
Malfunction ·ORASURE TECHNOLOGIES, INC.·Product code QKP·November 29, 2023

INTELISWAB COVID-19 RAPID TEST

FDA Adverse Event
Malfunction ·ORASURE TECHNOLOGIES, INC.·Product code QKP·November 29, 2023

ON-X ASCENDING AORTIC PROSTHESIS

FDA Adverse Event
Malfunction ·CRYOLIFE, INC. ¿ AUSTIN·Product code LWQ·October 4, 2016