Immunotech recalls Estrone RIA kits with specific lot numbers due to rare risk of false high results that could cause temporary injury. Affected kits may have inaccurate test results.
The affected Estrone RIA kit lots may rarely give falsely high patient results which might cause Temporary injury of Remote probability. Only in some (very rare) cases may the issue occur.
Immunotech recalls certain Estrone RIA test kits that may rarely give false high results, which could lead to temporary injury in very rare cases. This is a small risk that only affects specific lot numbers.
The affected kits may rarely produce false high results during testing. These false results could potentially cause temporary injury in very rare cases, but this is not a common issue.
People who own or use the Estrone RIA test kits with lot numbers 251013C (expiring Dec 2025) or 251110C (expiring Jan 2026) are affected. Those who use these kits for hormone testing are most at risk.
Check the lot number on the kit label. Affected lots are 251013C (expires Dec 2025) and 251110C (expires Jan 2026).
Look for the lot number on the kit label to determine if it's affected (251013C or 251110C).
The affected kits may rarely give false high results that could cause temporary injury in very rare cases, but this is not a common issue.
Check the lot number on the kit label. Affected lots are 251013C (expires Dec 2025) and 251110C (expires Jan 2026).
No, but you should check the lot number to see if your kit is affected. If it is, you may want to contact Immunotech for further instructions.
We’ve drafted a message you can send Immunotech to request your refund or repair — edit it as you like.
Subject: Recall Z-1369-2026 — Immunotech Immunotech Hello, I own a Immunotech that is covered by recall Z-1369-2026 from Immunotech. 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.
