125 results · 55ms · 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.

ESSURE

FDA Adverse Event
Injury ·BAYER PHARMA AG·Product code HHS·November 3, 2017

T:FLEX INSULIN DELIVERY SYSTEM

FDA Adverse Event
Injury ·TANDEM DIABETES CARE·Product code LZG·March 23, 2017

SYNVISC ONE

FDA Adverse Event
Injury ·GENZYME CORPORATION(RIDGEFIELD)·Product code MOZ·September 10, 2020

SCULPTRA, POLY-L-LACTIC ACID

FDA Adverse Event
Injury ·VALEANT USA·Product code LMH·January 8, 2014

ETHISORB DURA PATCH

FDA Adverse Event
Injury ·CODMAN & SHURTLEFF, INC.·Product code GXQ·August 25, 2016

ESSURE

FDA Adverse Event
Injury ·BAYER PHARMA AG·Product code HHS·March 20, 2019

ESSURE

FDA Adverse Event
Injury ·BAYER PHARMA AG·Product code HHS·September 21, 2020

SYNCHROMED II

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·February 21, 2020

ESSURE

FDA Adverse Event
Injury ·BAYER PHARMA AG·Product code HHS·November 24, 2017

ESSURE

FDA Adverse Event
Injury ·BAYER PHARMA AG·Product code HHS·October 31, 2017

ELECSYS ACTH TEST SYSTEM

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code CKG·November 21, 2016

CUSHING RONGEUR STR 2X10MM180MM

FDA Adverse Event
Malfunction ·AESCULAP AG·Product code HTX·November 6, 2019

ESSURE

FDA Adverse Event
Injury ·BAYER PHARMA AG·Product code HHS·February 20, 2017

PDSII VIO 27IN 4-0 S/A SH-1

FDA Adverse Event
Malfunction ·ETHICON INC.·Product code NEW·December 12, 2024

SYNVISC ONE

FDA Adverse Event
Injury ·GENZYME CORPORATION(RIDGEFIELD)·Product code MOZ·September 10, 2020

SYNVISC ONE

FDA Adverse Event
Injury ·GENZYME CORPORATION(RIDGEFIELD)·Product code MOZ·September 10, 2020

FLOSEAL

FDA Adverse Event
Injury ·BAXTER HEALTHCARE - HAYWARD·Product code LMF·July 6, 2015

ACUVUE OASYS BRAND

FDA Adverse Event
Injury ·VISTAKON·Product code LPL·March 25, 2014

SYNVISC ONE

FDA Adverse Event
Injury ·GENZYME CORPORATION(RIDGEFIELD)·Product code MOZ·September 10, 2020

Morph AccessPro Steerable Introducer; 6F Introducer, 45 cm working length Single use only. BioCardia, Inc. San Carlos, CA 94070 BioCardia Morph AccessPro is intended to provide a pathway through medical instruments cush as balloon dilation catheters, guidewires or other therapeutic devices that may be introduced into the peripheral vasculature.

FDA Recall
Terminated ·Biocardia, Inc.·Product code DYB·March 3, 2014