GET TESTED International AB recalls Menopause FSH 2 Tests due to distribution without premarket approval. All lots affected. Consumers should contact the company for details.
Distribution without premarket approval/clearance.
GET TESTED International AB has recalled all Menopause FSH 2 Tests products because they were distributed without proper regulatory approval. This recall is important because the tests may not meet safety standards.
The tests were distributed without premarket approval, meaning they weren't reviewed by regulatory authorities before being sold. This could lead to inaccurate results or health risks if used improperly.
Women who purchased the Menopause FSH 2 Tests from any retailer are affected. Those with medical conditions requiring hormone testing may be at higher risk.
Check for the EAN number 7340221700437 or SKU A-FSH on the product packaging. All lots of this test are affected.
Reach out to GET TESTED International AB for specific instructions on how to handle the recalled tests.
The tests were distributed without premarket approval, meaning they weren: t reviewed by regulatory authorities before being sold.
Look for the EAN number 7340221700437 or SKU A-FSH on the product packaging. All lots are affected.
Contact GET TESTED International AB for specific instructions on how to handle the recalled tests.
We’ve drafted a message you can send GET TESTED to request your refund or repair — edit it as you like.
Subject: Recall Z-0744-2026 — GET TESTED GET TESTED Hello, I own a GET TESTED that is covered by recall Z-0744-2026 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.
