161 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Recall
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Achilles Express Bone Sonometer
FDA Recall
Terminated
·GE Healthcare, LLC·Product code MUA·September 3, 2019
Achilles Insight Bone Sonometer
FDA Recall
Terminated
·GE Healthcare, LLC·Product code MUA·September 3, 2019
EvAir CPRSR Kit Upgrade: a) DISS/CEE 7/7 230V 50/60 HZ, Model Number M1230849; b) DISS/NEMA 5-15 115V 60 HZ, Model Number M1230847; c) NIST/BS 1363 230V 50/60 HZ, Model Number M1230849; d) NIST/BS 546 230V 50/60 HZ, Model Number M1230849; e) NIST/CEE 7/7 230V 50/60 HZ, Model Number M1230849;
FDA Recall
Open, Classified
·Datex-Ohmeda, Inc.·Product code BTI·December 29, 2023
IMMULITE/IMMULITE 1000 Systems TBG, catalog LKTB1 Quantitative measurement of Thyroxine-Binding Globulin (TBG) in serum, as an aid in the diagnosis and treatment of thyroid diseases.
FDA Recall
Terminated
·Siemens Healthcare Diagnostics, Inc.·Product code CEE·April 9, 2015
lnvatec SpA brand Diver C.E., Model/Catalog Numbers: DVR010014145, DVR011014145, Product is manufactured by lnvatec SpA, Roncadelle, Italy, and distributed by Invatec, Inc., Bethlehem, PA and by Medtronic Endovascular Therapies, Santa Rosa, CA The Diver C.E. product is an aspiration catheter indicated for the removal of fresh, soft emboli and thrombi from vessels in the arterial system.
FDA Recall
Terminated
·Invatec Llc·Product code DXE·March 4, 2009
Brand Name: CVS Honey Pad Product Name: CVS Honey Pad Model/Catalog Number: 9370613, 937404 Product Description: Infused with natural medical-grade honey Manuka (Leptospermum) honey is a medical-grade honey that is harvested from bees in New Zealand. Researchers have found that this species has unique components that make it ideal for wounds.
FDA Recall
Open, Classified
·Integra LifeSciences Corp. (NeuroSciences)·Product code FRO·August 5, 2025
Sofia 2 Analyzer Catalog Number 20299 Sofia 2 is a bench top analyzer intended to be used with Cassette-based immunofluorescent in vitro diagnostic assays . Sofia 2 is intended for professional and laboratory use.
FDA Recall
Terminated
·Quidel Corporation·Product code PSZ·December 15, 2017
BBL Columbia C.N.A. Agar w/5% Sheep Blood - Catalog Number 297831.
FDA Recall
Terminated
·Becton Dickinson & Co.·Product code JSO·July 2, 2004
Sheep Blood, Defibrinated - Catalog Number 212390, Unit 60 ml.
FDA Recall
Terminated
·Becton Dickinson & Co.·Product code JSO·July 2, 2004
Sheep Blood, Defibrinated - Catalog Number 211947, Unit 500 ml.
FDA Recall
Terminated
·Becton Dickinson & Co.·Product code JSO·July 2, 2004
BBL TSA II w/5% Sheep Blood, Spacesaver - Catalog Number 292537.
FDA Recall
Terminated
·Becton Dickinson & Co.·Product code JSO·July 2, 2004
Drager PT 4000 Phototherapy System
FDA Recall
Terminated
·Draeger Medical Systems, Inc.·Product code LBI·July 2, 2012
Sheep Blood, Defibrinated - Catalog Number 212389, Unit 30 ml.
FDA Recall
Terminated
·Becton Dickinson & Co.·Product code JSO·July 2, 2004
Sheep Blood, Defibrinated - Catalog Number 212391, Unit 250 ml.
FDA Recall
Terminated
·Becton Dickinson & Co.·Product code JSO·July 2, 2004
Sheep Blood, Defibrinated - Catalog Number 211945, Unit 15 ml.
FDA Recall
Terminated
·Becton Dickinson & Co.·Product code JSO·July 2, 2004
Sheep Blood, Defibrinated - Catalog Number 211946, Unit 100 ml.
FDA Recall
Terminated
·Becton Dickinson & Co.·Product code JSO·July 2, 2004
BBL Columbia C.N.A. Agar w/5% Sheep Blood/Levine EMB - Catalog Number 295618.
FDA Recall
Terminated
·Becton Dickinson & Co.·Product code JSO·July 2, 2004
BBL Brain Heart Infusion Agar CC w/Sheep Blood - Catalog Number 296178.
FDA Recall
Terminated
·Becton Dickinson & Co.·Product code JSO·July 2, 2004
BBL Brain Heart Infusion Agar w/10% Sheep Blood - Catalog Number 297655.
FDA Recall
Terminated
·Becton Dickinson & Co.·Product code JSO·July 2, 2004
PVA, PREVENT is an FDA-authorized emergency ventilator designed to treat patients suffering from COVID-19 respiratory failure. This motorized device automatically compresses a resuscitator bag to provide air to the lungs of a COVID-19 patient, eliminating the human error and fatigue that results from manual actuation. PREVENT is indicated for emergency resuscitation with appropriate patient monitoring on adult patients that require mechanical respiratory support.
FDA Recall
Open, Classified
·Precision Valve & Automation, Inc·Product code BTL·June 26, 2020