GET TESTED INTERNATIONAL AB recalls all Intestinal Worms Test products due to distribution without premarket approval. This may pose regulatory risks but does not indicate immediate safety hazards.
Distribution without premarket approval/clearance.
GET TESTED INTERNATIONAL AB is recalling all Intestinal Worms Test products because they were distributed without proper regulatory approval. This recall does not indicate an immediate safety risk to users.
The product was distributed without premarket approval or clearance from regulatory authorities. This means the product may not meet safety standards, but the recall does not describe specific safety hazards.
Anyone who purchased the Intestinal Worms Test product. The recall applies to all units sold globally.
Check for the product name 'Intestinal Worms Test' with EAN 616612785978 or SKU 2A169. All lots are affected.
Identify the product using the EAN 616612785978 or SKU 2A169.
The recall indicates distribution without premarket approval, but the official notice does not state that the product is unsafe for use.
The recall does not specify a need to stop using the product; it only notes distribution without regulatory approval.
The official notice does not mention replacement options or remedies.
We’ve drafted a message you can send GET TESTED INTERNATIONAL AB to request your refund or repair — edit it as you like.
Subject: Recall Z-0785-2026 — GET TESTED INTERNATIONAL AB GET TESTED INTERNATIONAL AB Hello, I own a GET TESTED INTERNATIONAL AB that is covered by recall Z-0785-2026 from GET TESTED INTERNATIONAL AB. 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.
