GET TESTED International AB recalls all Vitamin D-Test products distributed without premarket approval. Consumers should check product details for recall.
Distribution without premarket approval/clearance.
GET TESTED International AB is recalling all Vitamin D-Test products because they were distributed without proper premarket approval. This recall is due to regulatory compliance issues, though no specific safety risks are mentioned in the record.
The product was distributed without premarket approval, meaning it may not meet regulatory safety standards. This could lead to potential health risks if the test is not accurate or reliable. However, the recall record does not specify any actual safety hazards.
All owners of Vitamin D-Test products are affected. Individuals using these tests for health monitoring may be at risk due to regulatory compliance issues.
Check for the product name 'Vitamin D-Test' and the EAN number 7340221700802 or SKU A-VID. All lots of this product are affected.
Look for the EAN number 7340221700802 or SKU A-VID on the product label.
The product was distributed without premarket approval, which may not meet regulatory safety standards.
The recall record does not specify any safety hazards, so no immediate injury risk is mentioned.
Check for the EAN number 7340221700802 or SKU A-VID on the product label.
We’ve drafted a message you can send GET TESTED to request your refund or repair — edit it as you like.
Subject: Recall Z-0756-2026 — GET TESTED GET TESTED Hello, I own a GET TESTED that is covered by recall Z-0756-2026 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.
