Reported Nov 12, 2025 · Ongoing

Beckman Coulter UniCel DxI 600, Part Numbers: A71460, A30260; Photometric Chemistry Analyzer

Beckman Coulter, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Beckman Coulter, Inc. · 1000 Lake Hazeltine Dr · Chaska, MN · 55318-1037

Is this the product you have?

  • Beckman Coulter UniCel DxI 600
  • Part Numbers
    • A71460
    • A30260
    • Photometric Chemistry Analyzer
Lot codes and dates
    • A71460
    • UDI/DI 15099590369224
  • Serial Numbers
    • 902515
    • 902529
    • 902528
    • 902534
    • 902526
    • 902527
    • 902523
    • 902522
    • 902524
    • 902505
    • 902578
    • 902579
    • 902545
    • 902530
    • 902531
    • 902581
    • 902504
    • 902514
    • 902525
    • 902535
    • 902566
    • 902516
    • 902518
    • 902532
    • 902555
    • 902558
    • 902564
    • 902519
    • 902521
    • 902559
    • 902511
    • 902549
    • 902554
    • 902547
    • 902582
    • 902583
    • A30260
    • UDI/DI 15099590341602
  • Serial Numbers
    • 902536
    • 902541
    • 902517
    • 902563
    • 902565
    • 902557
    • 902513
    • 902507
    • 902543
    • 902560
    • 902562
    • 902506
    • 902508
    • 902574
    • 902533
    • 902572
    • 902540
    • 902569
    • 902568
    • 902577
    • 902510
    • 902580
    • 902567
    • 902573
    • 902570
    • 902571
    • 902538
    • 902553
    • 902552
    • 902512
    • 902539
    • 902561
    • 902575
    • 902544
    • 902542
    • 902556
    • 902537
    • 902509
    • 902520
    • 902546
    • 902548
    • 902551
    • 902550
    • 902576
Amount recalled
80 units

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Why it was recalled

An internal investigation has determined that due to defective sub-components within the gantry assembly, a z-axis CAD movement motion error may occur and cause an analyzer to enter a Not Ready or Paused state, leading to a delay in obtaining results.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:41 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.