Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

RESONATE EL ICD VR Recalled by Boston Scientific Corporation Due to The devices have an incorrect firmware configuration.

Date: October 4, 2017
Company: Boston Scientific Corporation
Status: Terminated
Source: FDA (Device)

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 Boston Scientific Corporation directly.

Affected Products

RESONATE EL ICD VR, Model D432, Sterile.

Quantity: 5 devices

Why Was This Recalled?

The devices have an incorrect firmware configuration.

Where Was This Sold?

This product was distributed to 2 states: MN, OH

Affected (2 states)Not affected

About Boston Scientific Corporation

Boston Scientific Corporation has 601 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report