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Beckman Coulter, Inc. recalls DxI 600 Access Immunoassay Analyzer W/Spot B, Part Number A71460
Recalled August 13, 2025 · FDA recall Z-2271-2025 · Beckman Coulter
Hazard
Beckman Coulter has identified that the UniCel DxI 600/800 systems with linear slide PnP gantries running software versions 5.7 and up faced incorrect PnP X-motor current settings where the PnP X-motor current incorrectly resets to 1.5A (instead of the required 2.0A) because the software overwrites the factory setting during installs or upgrades. This anomaly causes increased PnP motion errors which could lead to delays in reporting patient sample results if unnoticed. · FDA Class II
Units
177 systems
Sold at
Worldwide distribution - US Nationwide.
Description
Beckman Coulter has identified that the UniCel DxI 600/800 systems with linear slide PnP gantries running software versions 5.7 and up faced incorrect PnP X-motor current settings where the PnP X-motor current incorrectly resets to 1.5A (instead of the required 2.0A) because the software overwrites the factory setting during installs or upgrades. This anomaly causes increased PnP motion errors which could lead to delays in reporting patient sample results if unnoticed.
Product
DxI 600 Access Immunoassay Analyzer W/Spot B, Part Number A71460
Manufacturer(s)
Beckman Coulter, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →