Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
AutoMate 2500 Family Catalog No. ODL25120 AutoMate 1200 Recalled by Beckman Coulter Inc. Due to Beckman Coulter initiated a design change to update...
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
AutoMate 2500 Family Catalog No. ODL25120 AutoMate 1200, ODL25125, AutoMate 1250, ODL25250 AutoMate 2500, ODL25255 Automate 2550. AutoMate 1200/1250/2500/2550 System Series is a semi-open, pre- and post-analytical sample processing and sorting system. The base system automates the sample sorting, decapping, and archiving process. Handling and sorting of samples includes automatic detection of the tube type and cap type (color). Optional features include an Aliquot Module for creation of labeled secondary tubes (including detection of the presence of adequate volume for the requested aliquots) and a Recapper Module to re-seal previously decapped tubes prior to archiving.
Quantity: 4 units
Why Was This Recalled?
Beckman Coulter initiated a design change to update the Automate PC image to accommodate the operating system change to Windows 10.
Where Was This Sold?
This product was distributed to 1 state: MD
About Beckman Coulter Inc.
Beckman Coulter Inc. has 241 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report