GET TESTED International AB recalls iodine test kits due to distribution without premarket approval. All units are affected.
Distribution without premarket approval/clearance.
GET TESTED International AB has recalled all iodine test kits because they were distributed without proper regulatory approval. This means the products may not be safe for use.
The test kits were distributed without approval from health authorities, which means they might not meet safety standards. This could lead to inaccurate results or health risks if used improperly.
Anyone who purchased the iodine test kits from any retailer. The risk is highest for users who rely on these tests for medical purposes.
Check for the product name 'Iodine Test' and the EAN number 616612785572 or SKU 1JO. All lots of this product are affected.
Look for the EAN number 616612785572 or SKU 1JO on the product label.
The iodine test kits were distributed without premarket approval from health authorities, which may mean they don't meet safety standards.
Check for the EAN number 616612785572 or SKU 1JO on the product label. All lots of this product are affected.
The recall record does not specify a remedy, so you should contact the manufacturer directly for guidance.
We’ve drafted a message you can send GET TESTED to request your refund or repair — edit it as you like.
Subject: Recall Z-0810-2026 — GET TESTED GET TESTED Hello, I own a GET TESTED that is covered by recall Z-0810-2026 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.
