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

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

SECA

FDA Adverse Event
Malfunction ·SECA GMBH CO. KG·Product code FRI·April 14, 2023

SECA

FDA Adverse Event
Malfunction ·SECA CORP·Product code FRW·March 7, 2018

SECA

FDA Adverse Event
Malfunction ·SECA CORP.·Product code FRW·October 14, 2015

SECA

FDA Adverse Event
Malfunction ·SECA CORP.·Product code FRW·October 14, 2015

SECA 703

FDA Adverse Event
Malfunction ·SECA CORP.·Product code FRI·February 12, 2020

SECA 284

FDA Adverse Event
Malfunction ·SECA·Product code FRI·April 23, 2024

SECA 403 BABY SCALE CART

FDA Adverse Event
Malfunction ·SECA·Product code FRW·October 29, 2020

SECA 333

FDA Adverse Event
Malfunction ·SECA·Product code FRW·May 6, 2025

331I SECA SCALE

FDA Adverse Event
Malfunction ·SECA·Product code FRW·January 22, 2026

SECA 286

FDA Adverse Event
Malfunction ·SECA CORP.·Product code FRI·September 6, 2018

SCALE

FDA Adverse Event
Malfunction ·SECA CORP.·Product code FRW·October 16, 2015

PT2 GUIDE WIRE

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·March 8, 2010

CYPHER SIROLIMUS-ELUTING CORONARY STENT

FDA Adverse Event
Injury ·CORDIS DE MEXICO·Product code NIQ·September 13, 2007

VITALITY AVT

FDA Adverse Event
Malfunction ·CARDIAC PACEMAKERS, INC·Product code LWS·May 9, 2006

CYPHER SIROLIMUS-ELUTING CORONARY STENT

FDA Adverse Event
Injury ·CORDIS DE MEXICO·Product code NIQ·July 31, 2006

CONCERTO CRT-D DR

FDA Adverse Event
Injury ·MEDTRONIC MED REL, INC.·Product code NIK·February 9, 2010

CYPHER SIROLIMUS-ELUTING CORONARY STENT

FDA Adverse Event
Malfunction ·CORDIS DE MEXICO·Product code NIQ·April 9, 2007

PROMUS PREMIER

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NIQ·March 21, 2024

GREENLIGHT MOXY FIBER OPTIC

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code GEX·November 18, 2019

VITALITY AVT

FDA Adverse Event
Malfunction ·CARDIAC PACEMAKERS, INC·Product code LWS·May 9, 2006