International Medical Devices Database

Data Source

Country

Device Classification

Parent Company

Device Recall St. Jude Medical

Model / Serial
Integrity ADx DR Model 5360 & 5366 Identity ADx DR model 5286, 5380, 5386 &5480 Verity ADx DR 5256, 5356 & 5456
Product Classification
Cardiovascular Devices
Device Class
3
Implanted device?
Yes
Distribution
Nationwide and to four VA Medical Centers in IA and MO.
Product Description
Pulse Generator
Manufacturer
St Jude Medical
1 Event
- Recall of Device Recall St. Jude Medical

Eon model 65-3716, Eon Mini model 65-3788 and Brio model 65-6788, St. Jude Medical

Model / Serial
Implanted device?
Yes
Product Description
Active implantable medical devices - biostimulators
Manufacturer
St. Jude Medical
1 Event
- Field Safety Notices about Eon model 65-3716, Eon Mini model 65-3788 and Brio model 65-6788, St. Jude Medical

St. Jude Medical Ellipse™, Fortify Assura™, Unify Assura™

Model / Serial
Implanted device?
Yes
Product Description
Active implantable medical devices - defibrillators
Manufacturer
St. Jude Medical
2 Events
- Field Safety Notices about St. Jude Medical Ellipse™, Fortify Assura™, Unify Assura™
- Field Safety Notices about St. Jude Medical Ellipse™, Fortify Assura™, Unify Assura™

St. Jude Medical ICD Photon

Model / Serial
Implanted device?
Yes
Product Description
Active implantable medical devices
Manufacturer
Photon Micro and Atlas
1 Event
- Field Safety Notices about St. Jude Medical ICD Photon

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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.