Aug 6, 2019 4:06 AM
Recall of Ellipse implantable cardioverter defibrillators by Abbott (formerly St. Jude Medical Inc.) due to exposed aluminum wires that may prevent defibrillation therapy.
More on the FDA website.
Aug 6, 2019 4:06 AM
Recall of Ellipse implantable cardioverter defibrillators by Abbott (formerly St. Jude Medical Inc.) due to exposed aluminum wires that may prevent defibrillation therapy.
More on the FDA website.