International Medical Devices Database

Data Source

Country

Device Classification

Parent Company

Name	Date	Date initiated	Country	Source
Recall of Device Recall ESSENTIO MRI EL DR Pacemaker		2017-12-07	United States	USFDA
Recall of Device Recall PROPONENT SR Pacemaker		2017-12-07	United States	USFDA
Recall of Device Recall PROPONENT DR Pacemaker		2017-12-07	United States	USFDA
Recall of Device Recall PROPONENT EL DR Pacemaker		2017-12-07	United States	USFDA
Recall of Device Recall PROPONENT VDD SL Pacemaker		2017-12-07	United States	USFDA
Recall of Device Recall PROPONENT MRI Pacemaker		2017-12-07	United States	USFDA
Recall of Device Recall Ellipse		2016-03-31	United States	USFDA
Recall of Device Recall HeartMate II Left Ventricular Assist System (LVAS) with Pocket Controller		2017-03-30	United States	USFDA
Recall of Device Recall HeartMate II Left Ventricular Assist System (LVAS) with Pocket Controller		2017-03-30	United States	USFDA
Recall of Device Recall HeartMate II Left Ventricular Assist System (LVAS) with Pocket Controller		2017-03-30	United States	USFDA
Recall of Device Recall ACCOLADE SR Pacemaker		2017-12-07	United States	USFDA
Recall of Device Recall ACCOLADE DR Pacemaker		2017-12-07	United States	USFDA
Recall of Device Recall ACCOLADE EL DR Pacemaker		2017-12-07	United States	USFDA
Recall of Device Recall ACCOLADE MRI SR Pacemaker		2017-12-07	United States	USFDA
Recall of Device Recall ACCOLADE MRI DR Pacemaker		2017-12-07	United States	USFDA
Recall of Device Recall ALTRUA 2 EL DR Pacemaker		2017-12-07	United States	USFDA
Recall of Device Recall VISIONIST CRTP Pacemaker		2017-12-07	United States	USFDA
Recall of Device Recall VISIONIST X4 CRTP Pacemaker		2017-12-07	United States	USFDA
Recall of Device Recall ESSENTIO SR Pacemaker		2017-12-07	United States	USFDA
Recall of Device Recall ESSENTIO DR Pacemaker		2017-12-07	United States	USFDA
Recall of Device Recall ESSENTIO MRI SR Pacemaker		2017-12-07	United States	USFDA
Recall of Device Recall ESSENTIO MRI DR Pacemaker		2017-12-07	United States	USFDA
Recall of Device Recall ESSENTIO EL DR Pacemaker		2017-12-07	United States	USFDA
Recall of Device Recall AngioSeal		2006-06-07	United States	USFDA
Field Safety Notices about Ellipse DR, VR	2014-08-19		Serbia	ALIMSA

About this database

Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

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Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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The International Medical Devices Database is licensed under the Open Database License and its contents under Creative Commons Attribution-ShareAlike license. Always cite the International Consortium of Investigative Journalists when using this data. You can download a raw copy of the database here.

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