Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Siemens ADVIA Centaur Enhance Estradiol Test Code eE2 Catalog Number: 10490889 Recalled by Siemens Healthcare Diagnostics, Inc Due to The drug fulvestrant (Faslodex¿) may cause falsely elevated...
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
Siemens ADVIA Centaur Enhance Estradiol Test Code eE2 Catalog Number: 10490889, 10491445, 10697757 Product Usage: For in vitro diagnostic use in the quantitative determination of estradiol in human serum and plasma (heparinized and EDTA) using the ADVIA Centaur¿, ADVIA Centaur XP, ADVIA Centaur XPT and ADVIA Centaur CP systems.
Quantity: 33604 units
Why Was This Recalled?
The drug fulvestrant (Faslodex¿) may cause falsely elevated estradiol results.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Siemens Healthcare Diagnostics, Inc
Siemens Healthcare Diagnostics, Inc has 118 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report