FDAJune 29, 2017device

EMBLEM MRI S-ICD Model 219, Subcutaneous-Implantable Cardioverter Defibrillator, Rx. Product Usage: The S-ICD system is intended to provide defibrillation therapy for the treatment of life-threatening ventricular tachyarrhythmias in patients who do not have symptomatic bradycardia, incessant vent...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

The device can deliver an atypical amount of energy due to memory corruption inside the device.

What to do

FDA enforcement status: Terminated

Brands named

boston scientificboston

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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