PlainRecalls
FDA Devices Moderate Class II Ongoing

DxI 600 Access Immunoassay Analyzer W/Spot B, Part Number A71460

Reported: August 13, 2025 Initiated: June 25, 2025 #Z-2271-2025

Product Description

DxI 600 Access Immunoassay Analyzer W/Spot B, Part Number A71460

Reason for Recall

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.

Details

Recalling Firm
Beckman Coulter, Inc.
Units Affected
177 systems
Distribution
Worldwide distribution - US Nationwide.
Location
Chaska, MN

Frequently Asked Questions

What product was recalled?
DxI 600 Access Immunoassay Analyzer W/Spot B, Part Number A71460. Recalled by Beckman Coulter, Inc.. Units affected: 177 systems.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on August 13, 2025. Severity: Moderate. Recall number: Z-2271-2025.