13 results · 23ms · Sources: EU EUDAMED, US FDA

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VERTE-STACK K030736, K041197

FDA Adverse Event
Death ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code MQP·January 4, 2019

MOSAIC

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES DIVISION·Product code DYE·March 12, 2019

MONITOR, 100CC BURETTE W/ACORN FILTER

FDA Adverse Event
Malfunction ·INTEGRA NEUROSCIENCES PR·Product code FPA·July 20, 2006

CORNERSTONE-SR CAGE SYSTEM

FDA Adverse Event
Death ·MSD DEGGENDORF MFG·Product code ODP·February 17, 2012

HANCOCK II AORTIC BIOPROSTHETIC HEART VALVE

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES DIVISION·Product code DYE·May 27, 2020

ASR ACETABULAR IMPLANT 52

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL·Product code KWA·April 16, 2013

ANIMAS INSULIN INFUSION PUMP

FDA Adverse Event
Injury ·ANIMAS CORP.·Product code LZG·April 4, 2011

RX ACCULINK CAROTID STENT SYSTEM

FDA Adverse Event
Injury ·ABBOTT VASCULAR-VASCULAR SOLUTIONS·Product code NIM·June 16, 2008

MEDTRONIC SURGICAL ANNULOPLASTY PRODUCTS

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES DIVISION·Product code KRH·June 11, 2021

CG COMPOSITE RING

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES DIVISION·Product code KRH·September 2, 2020

DURAN ANCORE RING

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES DIVISION·Product code KRH·September 2, 2020

MEDTRONIC SURGICAL ANNULOPLASTY PRODUCTS

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES DIVISION·Product code KRH·May 16, 2023

CG COMPOSITE RING

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES DIVISION·Product code KRH·February 8, 2023