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

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UTERINE ARTERY EMBOLIZATION

FDA Adverse Event
Other ·*·Product code NAJ·December 15, 2004

UTERINE ARTERY EMBOLIZATION

FDA Adverse Event
Other ·*·Product code NAJ·August 30, 2006

ESSURE

FDA Adverse Event
Injury ·BAYER·Product code HHS·October 21, 2013

NOVASURE

FDA Adverse Event
Injury ·HOLOGIC·Product code MNB·September 21, 2015

V-LOC 180 ABS CLOS DEVICE 3-0 CL 18 P-12

FDA Adverse Event
Injury ·UNITED STATES SURGICAL·Product code GAM·October 5, 2010

SYNCHROMED II

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·May 31, 2022

NOVASURE IMPEDANCE CONTROLLED EA SYSTEM

FDA Adverse Event
Injury ·HOLOGIC, INC·Product code MNB·November 24, 2015

DISSQUICK CONNECT

FDA Adverse Event
Malfunction ·ABBOTT LABS·Product code LRQ·March 22, 2004

MICRO TIP WIPE

FDA Adverse Event
Injury ·DEVON INDUSTRIES INC·Product code LRQ·September 5, 2000

PORTABLE AC/DC SUCTION MACHINE

FDA Adverse Event
Malfunction ·VEGA TECHNOLOGIES / DICKSON ASIA GROUP, LTD.·Product code LRQ·September 25, 2024

@TRAY, TRACHEOSTOMY, BASIC, 4 GAU

FDA Adverse Event
Other ·MEDLINE INDUSTRIES, INC.·Product code LRQ·May 6, 2009

STND TRACH CARE TRAY W/PROXDE

FDA Adverse Event
Malfunction ·TYCO HEALTHCARE/KENDALL·Product code LRQ·February 8, 2007

TRACHEOSTOMY CLEANING TRAY/WITH GLOVES

FDA Adverse Event
Injury ·BAXTER·Product code LRQ·April 27, 1993

NA

FDA Adverse Event
UNK·Product code LRQ·August 24, 2004

PORTABLE AC/DC SUCTION MACINE

FDA Adverse Event
Malfunction ·VEGA TECHNOLOGIES/DICKSON ASIAN GROUP LTD.·Product code LRQ·August 25, 2025

PORTABLE AC/DC SUCTION MACHINE

FDA Adverse Event
Malfunction ·VEGA TECHNOLOGIES / DICKSON ASIA GROUP, LTD.·Product code LRQ·April 6, 2023

TRACH CARE TRAY STANDARD

FDA Adverse Event
KENMEX·Product code LRQ·May 12, 2004

TRACH CARE TRAY STANDARD

FDA Adverse Event
Death ·TYCO/KENDALL HEALTHCARE·Product code LRQ·September 12, 2005

TRACHEOSTOMY CARE TRAY

FDA Adverse Event
Malfunction ·KENDALL·Product code LRQ·October 2, 1998

*

FDA Adverse Event
Malfunction ·Product code LRQ·December 31, 1998