Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Ellipse ICD (Implantable Cardioverter Defibrillator) Model CD2411-36Q Recalled by St Jude Medical Inc. Due to St. Jude Medical is recalling the Ellipse ICD...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact St Jude Medical Inc. directly.
Affected Products
Ellipse ICD (Implantable Cardioverter Defibrillator) Model CD2411-36Q, CD2411-36C, CD1411-36Q, CD1411-36C Product Usage: Ellipse ICD devices are intended to provide ventricular antitachycardia pacing and ventricular defibrillation for automated treatment of life-threatening ventricular arrhythmias.
Quantity: 127 units
Why Was This Recalled?
St. Jude Medical is recalling the Ellipse ICD (Implantable Cardioverter Defibrillator) due to the potential inability to deliver high voltage therapy.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About St Jude Medical Inc.
St Jude Medical Inc. has 36 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report