Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Siemens Healthcare Diagnostics ADVIA Centaur Calibrator E - 2-Pack Catalog Recalled by Siemens Healthcare Diagnostics, Inc Due to ADVIA Centaur Systems Calibrator E Lot 42 and...
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 Healthcare Diagnostics ADVIA Centaur Calibrator E - 2-Pack Catalog Number: 04634452 SMN: 10309079 ADVIA Centaur¿ Calibrator E For in vitro diagnostic use in calibration the following assays using ADVIA Centaur systems: Cortisol, Progesterone Testosterone. ADVIA Centaur¿ Testosterone For in vitro diagnostic use in the quantitative determination of total testosterone {bound and unbound) in serum using the ADVIA Centaur and ADVIA Centaur XP Systems
Quantity: 15224 (2-pack)
Why Was This Recalled?
ADVIA Centaur Systems Calibrator E Lot 42 and 43 Bias with the Testosterone Assay
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