GET TESTED INTERNATIONAL AB recalls Neurotransmitters Plus due to distribution without premarket approval. All units are affected. No specific action steps provided in recall notice.
Distribution without premarket approval/clearance.
GET TESTED INTERNATIONAL AB has recalled all units of Neurotransmitters Plus because they were distributed without proper premarket approval. This means the product may not meet safety standards, but the recall does not specify a remedy or action for consumers.
The product was distributed without premarket approval, meaning it may not have undergone required safety testing before being sold. This could potentially lead to safety issues, but the recall does not specify what those issues are or how they might occur.
Anyone who owns or uses Neurotransmitters Plus. The risk is not clearly defined in the recall notice.
Neurotransmitters Plus with EAN: 616612786449 or SKU: F510. All lots of this product are affected.
Look for the EAN code 616612786449 or SKU F510 on the product label.
The product was distributed without premarket approval, which means it may not meet safety standards.
The recall notice does not specify any action steps for consumers.
The recall does not describe specific safety risks or hazards.
We’ve drafted a message you can send GET TESTED to request your refund or repair — edit it as you like.
Subject: Recall Z-0790-2026 — GET TESTED GET TESTED Hello, I own a GET TESTED that is covered by recall Z-0790-2026 from GET TESTED. 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.
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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.
