Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Abbott Alinity i Estradiol Reagent Kit - Product Usage: Alinity Recalled by Abbott Ireland Diagnostics Division Due to Patient results may be falsely elevated. This patient...
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 Abbott Ireland Diagnostics Division directly.
Affected Products
Abbott Alinity i Estradiol Reagent Kit - Product Usage: Alinity i Estradiol assay is a chemiluminescent microparticle immunoassay (CMIA) used for the quantitative The determination of Estradiol in serum and plasma on the Alinity i analyzer.
Quantity: 64,618
Why Was This Recalled?
Patient results may be falsely elevated. This patient impact only applies to patients currently being treated with or recently treated with the drug Mifepristone.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Abbott Ireland Diagnostics Division
Abbott Ireland Diagnostics Division has 12 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report