GET TESTED INTERNATIONAL AB recalls all Sperm Test products due to distribution without premarket approval. Consumers should contact the company for details.
Distribution without premarket approval/clearance.
GET TESTED INTERNATIONAL AB has recalled all Sperm Test products because they were distributed without proper regulatory approval. This recall does not pose an immediate safety risk but requires consumers to check if they have the product.
The product was distributed without premarket approval or clearance from regulatory authorities. This means the product may not meet safety standards, but the recall does not indicate an immediate risk of injury or harm.
Anyone who purchased the Sperm Test product from any retailer. People who have the product are most at risk of receiving it without proper regulatory clearance.
The product is labeled 'Sperm Test' with EAN 7340221700444 and SKU A-SPE. All lots of this product are affected.
Look for the EAN 7340221700444 and SKU A-SPE on the product label.
The recall indicates the product was distributed without premarket approval, but the official notice does not state if it is unsafe to use.
The product is labeled 'Sperm Test' with EAN 7340221700444 and SKU A-SPE. All lots are affected.
The official notice does not specify a remedy, so contact GET TESTED INTERNATIONAL AB for further 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-0750-2026 — GET TESTED GET TESTED Hello, I own a GET TESTED that is covered by recall Z-0750-2026 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.
