Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ADVIA¿ 120/2120/2120i 3-in-1 TESTpoint Control (ABN2 Control) Recalled by Siemens Healthcare Diagnostics, Inc. Due to Products have the incorrect platelet (PLT) value assignments...
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¿ 120/2120/2120i 3-in-1 TESTpoint Control (ABN2 Control)
Quantity: 3,266 units
Why Was This Recalled?
Products have the incorrect platelet (PLT) value assignments for the ADVIA 120/2120/2120i Hematology Systems.
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