15 results · 46ms · Sources: EU EUDAMED, US FDA

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KYPHON XPEDE BONE CEMENT

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NDN·December 21, 2018

KYPHON XPEDE BONE CEMENT

FDA Adverse Event
Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NDN·May 29, 2019

KYPHON XPEDE BONE CEMENT

FDA Adverse Event
Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code NDN·February 28, 2019

KYPHON XPEDE BONE CEMENT

FDA Adverse Event
Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code NDN·February 28, 2019

1030489-2019-01511

FDA Adverse Event
Death ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NDN·December 31, 2019

1030489-2019-01423

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code NDN·December 13, 2019

KYPHX® HV-R¿ BONE CEMENT

FDA Adverse Event
Malfunction ·CARDIAC SURGERY MFG KERKRADE·Product code NDN·September 8, 2021

KYPHX® HV-R¿ BONE CEMENT

FDA Adverse Event
Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NDN·July 22, 2022

KYPHON XPEDE BONE CEMENT

FDA Adverse Event
Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NDN·January 16, 2020

KANGAROO

FDA Adverse Event
Malfunction ·CARDINAL HEALTH 200, LLC·Product code KNT·October 16, 2024

ACCU-CHEK ® MULTICLIX

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·July 15, 2011

POLYFORM SYNTHETIC MESH

FDA Adverse Event
Injury ·PROXY BIOMEDICAL LTD.·Product code OTO·May 28, 2013

CAPSUREFIX NOVUS

FDA Adverse Event
Malfunction ·MPRI·Product code DTB·October 10, 2014

CHROMID STREPTO B AGAR

FDA Adverse Event
Malfunction ·BIOMERIEUX SA·Product code PQZ·November 1, 2017

CHROMID STREPTO B AGAR

FDA Adverse Event
Malfunction ·BIOMERIEUX SA·Product code PQZ·November 1, 2017