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Beckman Coulter Inc. recalls AutoMate 2500 Family Catalog No. ODL25120 AutoMate 1200, ODL25125, AutoMate 1250, ODL25250 AutoMate 2500, ODL25255 Autom
Recalled January 25, 2017 · FDA recall Z-1040-2017 · Beckman Coulter
Hazard
Beckman Coulter initiated a design change to update the Automate PC image to accommodate the operating system change to Windows 10. · FDA Class III
Units
4 units
Sold at
US Distribution to MD only.
Description
Beckman Coulter initiated a design change to update the Automate PC image to accommodate the operating system change to Windows 10.
Product
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.
Manufacturer(s)
Beckman Coulter Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →