Class II โ€” Potential Health Hazard

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

activator concentrate Recalled by Ecometics, Inc. Due to CGMP Deviations: Products not manufactured under current good...

Date: August 9, 2023
Company: Ecometics, Inc.
Status: Completed
Source: FDA (Drug)

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 Ecometics, Inc. directly.

Affected Products

activator concentrate, Sodium Fluoride 0.96% in Activator Concentrate; 0.08% in diluted Activator Solution, Net 1 FL. OZ., Manufactured for: All USA Direct, LLC, Broadview, IL 60155.

Quantity: 32,583 bottles

Why Was This Recalled?

CGMP Deviations: Products not manufactured under current good manufacturing practices.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Ecometics, Inc.

Ecometics, Inc. has 14 total recalls tracked by RecallDetector.

Related Recalls

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