GET TESTED International AB recalls all Liver Test products due to distribution without premarket approval. Consumers should contact the company for details on affected items and next steps.
Distribution without premarket approval/clearance.
GET TESTED International AB is recalling all Liver Test products because they were distributed without proper premarket approval. This recall is about regulatory compliance, not a safety hazard for users.
The product was distributed without approval from health authorities, which means it may not meet safety standards. However, this does not pose a direct risk to users during normal use.
Anyone who purchased the Liver Test product from any retailer. The risk is low as this is a regulatory issue, not a direct safety hazard.
The Liver Test product with EAN 7340221701724 and SKU D-LIV. All lots are affected, so there is no specific serial number or date range to check.
Reach out to GET TESTED International AB for specific instructions on how to handle the product.
No, this recall is due to regulatory compliance issues, not a safety hazard. The product is safe to use but must be handled according to the recall instructions.
Look for the Liver Test product with EAN 7340221701724 and SKU D-LIV. All lots are affected.
Contact GET TESTED International AB for specific instructions on how to handle the product.
We’ve drafted a message you can send GET TESTED to request your refund or repair — edit it as you like.
Subject: Recall Z-0801-2026 — GET TESTED GET TESTED Hello, I own a GET TESTED that is covered by recall Z-0801-2026 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.
