GET TESTED International Vaginal PH Test Recall: Distribution Without Premarket Approval

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Recalling firmGET TESTED INTERNATIONAL AB59334 Vastervik, Lysingsvagen 18 · Vastervik, N/A

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✎ GovInfoNow plain-language explainer

What happened, in plain English

GET TESTED International is recalling all Vag:PH tests because they were distributed without proper regulatory approval. This could pose risks if used without proper safety checks.

Why it’s dangerous

The product was distributed without premarket approval, meaning it hasn't been tested or approved by regulatory authorities before being sold. This could lead to potential safety issues if the test is used without proper validation.

Who’s affected

Anyone who purchased the Vaginal PH Test from a retailer. Women using the test for self-testing may be at risk.

How to tell if you have this one

The product is labeled as 'Vaginal PH Test' with EAN 7340221700680 and SKU A-PHV. All lots are affected.

Brand
GET TESTED
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Contact Manufacturer
Reach out to GET TESTED International for specific instructions on how to handle the recalled product.

✎ GovInfoNow

Questions people ask

Is this product safe to use?

The recall record states the product was distributed without premarket approval, but does not confirm if it is safe to use.

How can I check if I have the recalled product?

Look for the product labeled 'Vaginal PH Test' with EAN 7340221700680 and SKU A-PHV; all lots are affected.

What should I do if I have this product?

Contact GET TESTED International for specific instructions on handling the recalled product.

Take action

Contact GET TESTED

We’ve drafted a message you can send GET TESTED to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-0755-2026 — GET TESTED GET TESTED

Hello,

I own a GET TESTED that is covered by recall Z-0755-2026 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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Where this comes from

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.

Official source: FDA Recall #Z-0755-2026 (November 3, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0755-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

GET TESTED INTERNATIONAL AB recalls Vaginal PH Test

Recall notice