Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Beckman Coulter DxI 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due to A software error caused an increase in tray...
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 Beckman Coulter, Inc. directly.
Affected Products
Beckman Coulter DxI 9000 Access Immunoassay Analyzer, catalog number C11137; in-vitro diagnostic instrument
Quantity: 61 units
Why Was This Recalled?
A software error caused an increase in tray gripper motion errors that causes intermittent hard stops and a delay in patient results.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Beckman Coulter, Inc.
Beckman Coulter, Inc. has 79 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report