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  • Device 3309
  • Manufacturer 731
  • Event 124969
  • Implant 166
Name Classification Manufacturer Risk Class Country Source
Merlin PCS Programmer Software Cardiovascular Devices St Jude Medical Inc. 2 United States USFDA
Merlin PCS Programmer Software Cardiovascular Devices St Jude Medical Inc. 2 United States USFDA
Device Recall SUPERA VERITAS Gastroenterology-Urology Devices IDEV Technologies, Inc. 2 United States USFDA
Device Recall Percutaneous Trial Lead Kits Neurological Devices St. Jude Medical, Inc. 2 United States USFDA
Device Recall Percutaneous Trial Lead Kits Neurological Devices St. Jude Medical, Inc. 2 United States USFDA
Device Recall SwiftLock Anchor, Model 1192 Neurological Devices Advanced Neuromodulation Systems, Inc 2 United States USFDA
Device Recall HeartMate II Left Ventricular Assist System (LVAS) with Pocket Controller Cardiovascular Devices Thoratec Corporation 3 United States USFDA
Device Recall Proclaim Elite SCS IPG Neurological Devices St. Jude Medical, Inc. 3 United States USFDA
Device Recall Infinity DBS IPG Neurological Devices St. Jude Medical, Inc. 3 United States USFDA
Device Recall Infinity DBS IPG with MDT header Neurological Devices St. Jude Medical, Inc. 3 United States USFDA
Device Recall Infinity DBS IPG Neurological Devices St. Jude Medical, Inc. 3 United States USFDA
Device Recall Infinity DBS IPG with MDT header Neurological Devices St. Jude Medical, Inc. 3 United States USFDA
Device Recall Merlinhome RF Remote Monitoring Transmitter, Model EX1150, with software versions 6.1M or 7.0 Cardiovascular Devices St Jude Medical Cardiac Rhythm Management Division 3 United States USFDA
Device Recall Unify and Unify Assura Cardiovascular Devices St Jude Medical Inc. 3 United States USFDA
Device Recall Anthem, Allure Cardiovascular Devices St Jude Medical Inc. 3 United States USFDA
Device Recall Assurity, Assurity Cardiovascular Devices St Jude Medical Inc. 3 United States USFDA
Device Recall Assurity MRI Cardiovascular Devices St Jude Medical Inc. 3 United States USFDA
Device Recall Merlin Patient Care System Cardiovascular Devices St Jude Medical Inc. 3 United States USFDA
Device Recall MerlinHome Cardiovascular Devices St Jude Medical Inc. 3 United States USFDA
Device Recall Fortify, Fortify Assura Cardiovascular Devices St Jude Medical Inc. 3 United States USFDA
Device Recall Optisure HV lead Cardiovascular Devices St Jude Medical Cardiac Rhythm Management Division 3 United States USFDA
Device Recall MitraClip Clip Delivery System Cardiovascular Devices Abbott Vascular 3 United States USFDA
Device Recall Ellipse Cardiovascular Devices St Jude Medical Inc. 3 United States USFDA
Device Recall HeartMate II Left Ventricular Assist System (LVAS) with Pocket Controller Cardiovascular Devices Thoratec Corporation 3 United States USFDA
Device Recall HeartMate II Left Ventricular Assist System (LVAS) with Pocket Controller Cardiovascular Devices Thoratec Corporation 3 United States USFDA
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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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