31 results · 43ms · Sources: EU EUDAMED, US FDA

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ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code HSB·December 18, 2014

ESSURE

FDA Adverse Event
Injury ·BAYER PHARMA AG·Product code HHS·May 10, 2023

BD MAXZERO MULTI-FUSE EXTENSION SET WITH NEEDLELESS CONNECTOR

FDA Adverse Event
Malfunction ·SISTEMAS MEDICOS ALARIS S.A. DE C.V.·Product code FPA·September 27, 2024

BD MAXZERO MULTI-FUSE EXTENSION SET WITH NEEDLELESS CONNECTOR

FDA Adverse Event
Malfunction ·SISTEMAS MEDICOS ALARIS S.A. DE C.V.·Product code FPA·October 30, 2024

BKS UNI

FDA Adverse Event
Injury ·ORTHO DEVELOPMENT·Product code HSX·August 4, 2022

BKS HIGH FLEX

FDA Adverse Event
Injury ·ORTHO DEVELOPMENT CORP.·Product code JWH·May 13, 2014

BKS HIGH FLEX

FDA Adverse Event
Injury ·ORTHO DEVELOPMENT CORP.·Product code JWH·May 13, 2014

NITE GUARD

FDA Adverse Event
Malfunction ·RANIR LLC·Product code OBR·May 1, 2014

KS PREMIUM TENS ELECTRODE PADS

FDA Adverse Event
Injury ·K.S. CHOI, CORPORATION·Product code GXY·July 2, 2025

MULTI-WAY CONNECTING SET 4 SS

FDA Adverse Event
Malfunction ·DKS LOVERSAN D.O.O.·Product code LHI·April 23, 2020

OTTR

FDA Adverse Event
Malfunction ·HKS MEDICAL INFO SYSTEMS·Product code LNX·February 16, 2010

PROLENE BLU 75CM 3-0 KS

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAW·February 5, 2024

MONOCRYL UND 70CM 2-0 KS

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAN·January 7, 2019

PROLENE BLUE 2-0 75CM 1 KS

FDA Adverse Event
Malfunction ·ETHICON INC.·Product code GAW·February 23, 2026

AMPLATZER PICCOLO

FDA Adverse Event
Injury ·ABBOTT MEDICAL·Product code MAE·March 25, 2022

IPRISM

FDA Adverse Event
Injury ·OCULAR INSTRUMENTS·Product code HKS·April 3, 2014

COBE

FDA Adverse Event
Injury ·COBE CAMBRO HOSPITAL·Product code JKS·March 7, 1994

VOLK SINGLE USE SLT LENS (DISPOSABLE)

FDA Adverse Event
Malfunction ·VOLK OPTICAL INC.·Product code HKS·April 28, 2026

*

FDA Adverse Event
Malfunction ·NEMSCHOFF·Product code FKS·September 11, 2011

IL 482 CO-OXIMETER

FDA Adverse Event
Malfunction ·INSTRUMENTATION LABORATORY CO.·Product code JKS·October 27, 2001