International Medical Devices Database

Data Source

Country

Device Classification

Parent Company

Name	Date initiated	Country	Source
Recall of Device Recall HeartMate II Left Ventricular Assist System (LVAS) with Pocket Controller	2017-03-30	United States	USFDA
Recall of Device Recall ALTRUA 2 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 HeartMate II Left Ventricular Assist System (LVAS) with Pocket Controller	2017-03-30	United States	USFDA
Recall of Device Recall ACCOLADE DR 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 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 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 ACCOLADE SR 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 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 ACCOLADE MRI EL DR Pacemaker	2017-12-07	United States	USFDA
Recall of Device Recall Merlinhome RF Remote Monitoring Transmitter, Model EX1150, with software versions 6.1M or 7.0	2014-12-18	United States	USFDA
Recall of Device Recall TactiSys Quartz Pack, PN004 400	2014-11-25	United States	USFDA
Recall of Device Recall Optisure HV lead	2015-11-03	United States	USFDA
Recall of Device Recall VALITUDE CRTP Pacemaker	2017-12-07	United States	USFDA
Recall of Device Recall VALITUDE X4 CRTP Pacemaker	2017-12-07	United States	USFDA
Recall of Device Recall ALTRUA 2 SR Pacemaker	2017-12-07	United States	USFDA
Recall of Device Recall ALTRUA 2 DR Pacemaker	2017-12-07	United States	USFDA
Recall of Device Recall VISIONIST CRTP Pacemaker	2017-12-07	United States	USFDA

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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.