Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
DxI 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due to the DxI 9000 encoder wheel was misaligned on...
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
DxI 9000 Access Immunoassay Analyzer, Catalog Number C11137.
Quantity: 206 units
Why Was This Recalled?
the DxI 9000 encoder wheel was misaligned on the motor shaft, leading to increased slippage errors and causing the instrument to stop, posing a high safety risk due to potential delays 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