FDA recall record

Beckman Coulter DxI 600 Access Immunoassay Analyzer W/Dual Gantry, Part Number A71461 recall — FDA Z-2270-2025

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…

Class IIclassification
Z-2270-2025official record ID
Aug 13, 2025report date

Recall record at a glance

Official recordZ-2270-2025
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmBeckman Coulter, Inc.
Report dateAug 13, 2025
Recall initiation dateJun 25, 2025
Quantity1 system
LocationChaska, MN, United States

Official product description

DxI 600 Access Immunoassay Analyzer W/Dual Gantry, Part Number A71461

Why the product was 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.

Distribution information

Worldwide distribution - US Nationwide.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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About this record

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