International safety notice
Safety Information for St. Jude Medical Ellipse™, Fortify Assura™, Unify Assura™, and Quadra Assura™ Implantable Cardioverter Defibrillators (ICDs) and Assurity™and Allure™ Pacemakers
Germany / BfArM · DEU · Jan 7, 2015
Key facts
| Title | Safety Information for St. Jude Medical Ellipse™, Fortify Assura™, Unify Assura™, and Quadra Assura™ Implantable Cardioverter Defibrillators (ICDs) and Assurity™and Allure™ Pacemakers |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | St. Jude Medical Ellipse™, Fortify Assura™, Unify Assura™, and Quadra Assura™ Implantable Cardioverter Defibrillators (ICDs) and Assurity™and Allure™ Pacemakers |
| Manufacturer | Safety Information for St. Jude Medical Ellipse™, Fortify Assura™, Unify Assura™, and Quadra Assura™ Implantable Cardioverter Defibrillators (ICDs) and Assurity™and Allure™ Pacemakers |
| Models | 55117, EX1150, 0.016 |
| Date | Jan 7, 2015 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers in FDA data
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1