Class II — Potential Health Hazard

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

Nicolet¿ Ambulatory EEG Recalled by Natus Neurology Inc Due to Potential to be able to import an ambulatory...

Date: February 1, 2018
Company: Natus Neurology Inc
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 Natus Neurology Inc directly.

Affected Products

Nicolet¿ Ambulatory EEG

Quantity: 171 units

Why Was This Recalled?

Potential to be able to import an ambulatory exam for a patient for which the exam was not started.

Where Was This Sold?

This product was distributed to 25 states: AZ, AR, CA, CO, FL, GA, ID, IL, IN, ME, MA, MI, MO, NV, NJ, NY, NC, ND, PA, TN, TX, VA, WA, WI, DC

Affected (25 states)Not affected

About Natus Neurology Inc

Natus Neurology Inc has 8 total recalls tracked by RecallDetector.

Related Recalls

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