GET TESTED International AB recalls GI Microbiome Profile Small products distributed without premarket approval. Consumers should check product details and contact the company for guidance.
Distribution without premarket approval/clearance.
GET TESTED International AB has recalled all GI Microbiome Profile Small products due to being distributed without premarket approval. This means the products were not approved by the FDA before being sold, which could pose safety risks.
Products distributed without premarket approval by the FDA may not meet safety standards. This could lead to potential health risks if the product is used without proper regulatory oversight.
Anyone who purchased the GI Microbiome Profile Small product from any retailer. People using the product for health testing may be at risk due to unapproved distribution.
Check for the product name 'GI Microbiome Profile Small' and the EAN code 7340221709195. All lots of this product are affected.
Look for the EAN code 7340221709195 on the product label to confirm it is affected.
The product was distributed without premarket approval by the FDA, meaning it was not approved for safety and effectiveness before being sold.
Check the product details to confirm it is affected; contact GET TESTED International AB for further guidance.
The recall notice does not specify a deadline for action.
We’ve drafted a message you can send GET TESTED to request your refund or repair — edit it as you like.
Subject: Recall Z-0763-2026 — GET TESTED GET TESTED Hello, I own a GET TESTED that is covered by recall Z-0763-2026 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.
