Class II — Potential Health Hazard

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

Abbott Aveir Leadless Pacemaker Recalled by Abbott Medical Due to Their is a potential that electromagnetic interference may...

Date: February 5, 2024
Company: Abbott Medical
Status: Ongoing
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 Abbott Medical directly.

Affected Products

Abbott Aveir Leadless Pacemaker, REF: LSP112V, STERILEEO

Quantity: 10,610 units

Why Was This Recalled?

Their is a potential that electromagnetic interference may cause leadless pacemaker may result in mode change.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Abbott Medical

Abbott Medical has 42 total recalls tracked by RecallDetector.

Related Recalls

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