Siemens Healthcare recalls ADVIA Centaur Enhanced Estradiol (eE2) 100T tests due to potential falsely elevated estradiol results, which could lead to misdiagnosis. All lots are affected.
Falsely Elevated Results Observed with Plasma Specimens, could lead a clinician to misinterpret patient results
Siemens Healthcare is recalling ADVIA Centaur Enhanced Estradiol (eE2) 100T tests because they may produce falsely high estradiol results. This could lead doctors to misinterpret patient results and make incorrect medical decisions.
The test may show higher estradiol levels than actually present in a patient's blood. This could cause doctors to misinterpret results and potentially make incorrect medical decisions about a patient's health.
Patients using the ADVIA Centaur eE2 100T test for estradiol measurement may be affected. Healthcare providers ordering the test are most at risk of misdiagnosis.
Check the lot number on the test kit. All lots of the ADVIA Centaur Enhanced Estradiol (eE2) 100T test are affected, including those with lot numbers listed in the recall notice.
Look for the lot number on the test kit to confirm if it is affected. All lots are included in this recall.
The test may produce falsely elevated estradiol results, which could lead doctors to misinterpret patient results.
All lots of the ADVIA Centaur Enhanced Estradiol (eE2) 100T test are affected. Check the lot number on the test kit.
Check the lot number on the test kit. If it is affected, contact Siemens Healthcare for guidance.
We’ve drafted a message you can send Siemens Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-1023-2022 — Siemens Healthcare Siemens Healthcare Hello, I own a Siemens Healthcare that is covered by recall Z-1023-2022 from Siemens Healthcare. 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.
