GET TESTED INTERNATIONAL AB recalls all DHEA Test products due to distribution without premarket approval. Consumers should contact the company for details.
Distribution without premarket approval/clearance.
GET TESTED INTERNATIONAL AB is recalling all DHEA Test products because they were distributed without proper premarket approval. This recall does not involve a safety hazard but addresses regulatory compliance issues.
The product was distributed without receiving premarket approval or clearance from regulatory authorities. This means the product may not meet safety or quality standards set by the government.
Anyone who purchased the DHEA Test product from any retailer. The risk is low as this is a regulatory compliance issue, not a safety hazard.
The DHEA Test product with EAN: 616612786418 and SKU: O320. All lots of this product are affected.
Reach out to GET TESTED INTERNATIONAL AB for specific instructions on what to do with the product.
No, this recall is for regulatory compliance reasons, not a safety hazard.
Look for the EAN: 616612786418 and SKU: O320 on the product label.
Contact GET TESTED INTERNATIONAL AB for specific instructions.
We’ve drafted a message you can send GET TESTED to request your refund or repair — edit it as you like.
Subject: Recall Z-0776-2026 — GET TESTED GET TESTED Hello, I own a GET TESTED that is covered by recall Z-0776-2026 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.
