76 results · 7ms · 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.

Draeger Jaundice Meter JM-105 The device is intended for use in hospitals, clinics or doctor s offices under a physician s supervision / direction to assist clinicians in monitoring of newborn infants. The device is not intended as a standalone for diagnosis of hyperbilirubinemia. It is to be used in conjunction with other clinical signs and laboratory measurements. The Jaundice Meter is not intended for home use. The Jaundice Meter may only be used at the sternum measurement site for Physician s office applications.

FDA Enforcement
Class I ·Terminated·Draeger Medical Systems, Inc.·June 13, 2018

Part 510636 Disposable Infusion Pump, ...Elastomeric Pump 600 mL( 300 ml perside), 2 to 10 ml/hr. Delivery time 60 to 144 hours; found in the following kits: GoBlock Kit 510646, Disposable Infusion Pump for drug delivery. Symbios GOBlock System is a disposable, self contained infusion system.

FDA Enforcement
Class I ·Terminated·Symbios Medical Products, LLC·June 12, 2013

NOxBOXi Nitric Oxide Delivery System; Model Numbers: NOXBOX-I

FDA Enforcement
Class I ·Ongoing·NOXBOX LTD·October 15, 2025

NOxBOXi Nitric Oxide Delivery System; Model Numbers: NOXBOX-I

FDA Enforcement
Class I ·Ongoing·NOXBOX LTD·October 15, 2025

ResMed Stellar, Non-invasive/invasive ventilators, Model: 100, 150

FDA Enforcement
Class I ·Completed·ResMed Ltd.·February 12, 2020

Ellume COVID-19 Home Test

FDA Enforcement
Class I ·Ongoing·ELLUME LTD·November 17, 2021

AirFit N10 Nasal Masks and User Guide

FDA Enforcement
Class I ·Ongoing·ResMed Ltd.·December 27, 2023

AirFit N20 Nasal Mask and User Guide

FDA Enforcement
Class I ·Ongoing·ResMed Ltd.·December 27, 2023

AirTouch N20 Nasal Mask and User Guide

FDA Enforcement
Class I ·Ongoing·ResMed Ltd.·December 27, 2023

AirFit F20 Full Face Mask and User Guide

FDA Enforcement
Class I ·Ongoing·ResMed Ltd.·December 27, 2023

Astral 100 and Astral 150 ventilators

FDA Enforcement
Class I ·Ongoing·ResMed Ltd.·November 1, 2023

AirFit F30 Full Face Mask and User Guide

FDA Enforcement
Class I ·Ongoing·ResMed Ltd.·December 27, 2023

AirTouch F20 Full Face Mask and User Guide

FDA Enforcement
Class I ·Ongoing·ResMed Ltd.·December 27, 2023

AirFit F30i Full Face Mask and User Guide

FDA Enforcement
Class I ·Ongoing·ResMed Ltd.·December 27, 2023

NOxBOXi Nitric Oxide Delivery System, NOXBOX-I, REQNOXBOX-I, Nitric Oxide Delivery Device

FDA Enforcement
Class I ·Terminated·NOXBOX LTD·June 21, 2023

Bravo CF capsule delivery device, designed to place and attach a pH monitoring capsule to the esophagus using endoscopic or manometric guidance, Product Number FGS-0635 (5 pack) and FGS-0636 (1 pack)

FDA Enforcement
Class I ·Ongoing·Given Imaging Ltd.·July 16, 2025

ProVu Single Use Video Stylet with ET Tube, Part/Size: 038-990-080U/ 8.0, 038-990-075U/ 7.5, 038-990-070U/ 7.0, 038-990-065U/ 6.5 *Note: product list updated per 12/23/2020 letter to customers

FDA Enforcement
Class I ·Terminated·Flexicare Medical Ltd.·December 2, 2020

ReSTOR intraocular lens and ReSTOR Toric intraocular lens. The Alcon AcrySof IQ ReSTOR and IQ ReSTOR Toric intraocular lenses are posterior chamber lenses intended as optical implants designed to replace the human crystalline lens in adult patients following cataract surgery. The lenses subject to this correction are manufactured specifically for Japan.

FDA Enforcement
Class I ·Terminated·Alcon Research, Ltd.·August 19, 2015

Inspiration Ventilator System, i Series and LS 12.1 LCD. The Inspiration 7i / 5i Ventilator System is to be used by healthcare professionals in hospitals or healthcare facilities and intra-hospital transport.

FDA Enforcement
Class I ·Terminated·Event Medical LTD·November 25, 2015

Expansion of previous recall of AcrySof IQ ReSTOR and AcrySof IQ ReSTOR Toric IOL; now to include AcrySof IQ Toric models SN6AT6, SN6AT7, SN6AT8, and SN6AT9. Intended for primary implantation in the capsular bag of the eye for visual correction.

FDA Enforcement
Class I ·Terminated·Alcon Research, Ltd.·December 2, 2015