93 results · 40ms · Sources: EU EUDAMED, US FDA

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CRITICAL DISPOSABLES

FDA Adverse Event
Malfunction ·DEROYAL·Product code DTI·March 22, 2001

CRITICAL DISPOSABLES

FDA Adverse Event
Malfunction ·DEROYAL·Product code BYX·April 19, 2001

ONE TOUCH ULTRA-MINI

FDA Adverse Event
Injury ·LIFESCAN·Product code NBW·December 5, 2017

RESTORE ULTRA

FDA Adverse Event
Malfunction ·MEDTRONIC NEUROMODULATION·Product code LGW·February 15, 2011

CYCLOSPORINE

FDA Adverse Event
Injury ·ROCHE - GMBH·Product code MKW·October 4, 2002

WESTERN MEDICA MEDICAL OXYGEN PRESET REGULATOR

FDA Adverse Event
Injury ·WESTERN/SCOTT FETZER CO.·Product code CAN·January 10, 2014

ACCU-CHEK COMFORT CURVE TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code NBW·October 25, 2006

RESTORE ADVANCED RECHARGEABLE

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO·Product code LGW·November 20, 2008

ACCU-CHEK ADVANTAGE

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code NBW·May 7, 2007

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Injury ·TANDEM DIABETES CARE·Product code QFG·July 21, 2025

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Injury ·TANDEM DIABETES CARE·Product code QFG·June 24, 2022

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Injury ·TANDEM DIABETES CARE·Product code QFG·September 5, 2025

T:SLIM X2 INSULIN PUMP WITH INTEROPERABLE TECHNOLOGY

FDA Adverse Event
Injury ·TANDEM DIABETES CARE·Product code QFG·September 5, 2024

BEAR III

FDA Adverse Event
Injury ·BEAR MEDICAL SYSTEMS, INC.·Product code CBK·November 22, 1996

IMPLANTABLE CARDIOVERTER DEFIBRILLATOR (NON-CRT)

FDA Adverse Event
Malfunction ·MEDTRONIC·Product code LWS·August 12, 2023

ENDOTAK ENDURANCE RX

FDA Adverse Event
Malfunction ·CARDIAC PACEMAKERS, INC·Product code DTB·November 14, 2005

VALITUDE CRT-P

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code NKE·May 1, 2023

VIGILANT EL ICD DR

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LWS·February 7, 2022

EZ STEER¿ NAV BI-DIRECTIONAL ELECTROPHYSIOLOGY CATHETER

FDA Adverse Event
Injury ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code LPB·December 16, 2013

HEARTMATE II LVAS

FDA Adverse Event
Injury ·THORATEC CORP.·Product code DSQ·November 14, 2013