Ecometics recalls activator concentrate with sodium fluoride due to manufacturing deviations. Products not made under current good manufacturing practices.
CGMP Deviations: Products not manufactured under current good manufacturing practices.
Ecometics is recalling activator concentrate products that were not made under current good manufacturing practices. This means the products may not meet safety standards and could pose risks.
The products were manufactured without following current good manufacturing practices. This could lead to inconsistent quality and potential safety issues with the sodium fluoride concentration.
Users of activator concentrate products made by Ecometics for dental use are affected. Those who have the specific product with lot number 1E175B are most at risk.
Check for the product name 'Activator Concentrate' with sodium fluoride 0.96% or 0.08% in diluted solution. The lot number 1E175B and expiration date 6/24 are specific identifiers.
Look for the lot number 1E175B and expiration date 6/24 on the product label.
The products were not manufactured under current good manufacturing practices, which could affect their safety and quality.
Check for the product name 'Activator Concentrate' with sodium fluoride 0.96% or 0.08% in diluted solution, lot number 1E175B, and expiration date 6/24.
The recall record does not specify a remedy, so contact Ecometics for further instructions.
We’ve drafted a message you can send Ecometics to request your refund or repair — edit it as you like.
Subject: Recall D-1100-2023 — Ecometics Ecometics Hello, I own a Ecometics that is covered by recall D-1100-2023 from Ecometics. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
