Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ADVIA 2120 Dual Aspirate Autosampler (SMN 10313419) - OUS Recalled by Siemens Healthcare Diagnostics, Inc. Due to Potential Sample Identification (SID) Mismatch with14-Character Barcodes
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 2120 Dual Aspirate Autosampler (SMN 10313419) - OUS, automated hematology analyzer Software Versions 6.10 and 6.11
Quantity: 283 units
Why Was This Recalled?
Potential Sample Identification (SID) Mismatch with14-Character Barcodes
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