Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ADVIA Centaur Enhanced Estradiol (eE2) 100T - In vitro diagnostic Recalled by Siemens Healthcare Diagnostics, Inc. Due to Falsely Elevated Results Observed with Plasma Specimens, could...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Siemens Healthcare Diagnostics, Inc. directly.
Affected Products
ADVIA Centaur Enhanced Estradiol (eE2) 100T - In vitro diagnostic use in the quantitative determination of estradiol SMN: 10490889 All lots
Quantity: 2,315 units
Why Was This Recalled?
Falsely Elevated Results Observed with Plasma Specimens, could lead a clinician to misinterpret patient results
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Siemens Healthcare Diagnostics, Inc.
Siemens Healthcare Diagnostics, Inc. has 452 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report