Reported May 25, 2022 · Ongoing

DxM 1040 MicroScan WalkAway Instrument REF B1018-440

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. · 250 S Kraemer Blvd · Brea, CA · 92821-6232

Is this the product you have?

  • DxM 1040 MicroScan WalkAway Instrument REF B1018-440
Lot codes and dates
  • Catalog NumberB1018-440
  • UDI-DI Code15099590690885
  • Serial Numbers
    • 44010026
    • 44010027
    • 44010028
    • 44010029
    • 44010030
    • 44010031
    • 44010032
    • 44010033
    • 44010035
    • 44010036
    • 44010037
    • 44010038
    • 44010040
    • 44010041
    • 44010042
    • 44010043
    • 44010044
    • 44010045
    • 44010046
    • 44010047
    • 44010048
    • 44010049
    • 44010050
    • 44010051
    • 44010052
    • 44010053
    • 44010054
    • 44010055
    • 44010056
    • 44010057
    • 44010058
    • 44010059
    • 44010060
    • 44010061
    • 44010063
    • 44010064
    • 44010065
    • 44010066
    • 44010067
    • 44010068
Amount recalled
40 systems

This recall covers 6 products

The agency filed one notice per product. You are reading one of them; the other 5 are below.

Where it was sold

Why it was recalled

WalkAway Instruments may have been assembled with the incorrect AC power entry connector inlet with is rated at 1 ampere current rating rather than the correct current rating of 10 ampere

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, 5:37 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.