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Recall Observatory FDA recall evidence

Device product

The SQ-RX Pulse Generator a component of the Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System 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 ventricular tachycardia, or spontaneous, frequently recurring ventricular tachycardia that is reliably terminated with anti-tachycardia pacing.

Z-0474-2019

November 01, 2018

Class II

Product summary

Firm
Boston Scientific Corporation
Event
Event 81471
Status
Terminated
Classification
Class II
Quantity
12,900
Official record key
device-enforcement:Z-0474-2019

Official wording

Reason: Experienced accelerated battery depletion and a shortened replacement interval due to latent internal battery malfunctions.

Code information: SQ-RX Pulse Generator Model 1010

Distribution pattern: US Nationwide Distribution: Alabama, Alaska, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, District of Columbia, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin, and Wyoming.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Experienced accelerated battery depletion and a shortened replacement interval due to latent internal battery malfunctions.