Product Advisories for the Ellipse ICD

Ellipse

Implantable Cardioverter Defibrillator

Product Advisories

Urgent Medical Device Recall: Ellipse Implantable Cardioverter Defibrillator (ICD) Latent Electronics Vulnerability – June 20, 2019

A product recall and a subsequently provided urgent medical device recall notice communicating patient management recommendations for a small number of Ellipse implantable cardioverter defibrillators which may be subject to a latent vulnerability in the electronics circuitry.

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MAT-2001111 v5.0

CARDIOVASCULAR

Ellipse

Implantable Cardioverter Defibrillator

Product Advisories

Urgent Medical Device Recall: Ellipse Implantable Cardioverter Defibrillator (ICD) Latent Electronics Vulnerability – June 20, 2019

Medical Device Advisory: Ellipse and Ellipse ST VR/DR ICD – August 19, 2014

POLICIES & ADVISORIES

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