Reported Apr 29, 2020 · Terminated

Beckman Coulter Power Express Sample Processing System AU5800XL connection unit, catalog #B36351; and Power Express…

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?

  • Beckman Coulter Power Express Sample Processing System AU5800XL connection unit, catalog #B36351; and Power Express Dynamic Inlet, catalog B36352.
Lot codes and dates
  • All serial
  • numbers installed before 5/20/2019

    92 of 92 codes

    • Serials numbers in the U.S.: PW211409002
    • PW211501005
    • PW211501006
    • PW211501007
    • PW211501008
    • PW211501013
    • PW211505001
    • PW211508003
    • PW211509002
    • PW211510001
    • PW211510002
    • PW211511001
    • PW211511002
    • PW211511003
    • PW211511005
    • PW211512001
    • PW211601001
    • PW211601002
    • PW211602002
    • PW211602003
    • PW211602004
    • PW211603001
    • PW211603002
    • PW211603003
    • PW211604001
    • PW211604002
    • PW211604005
    • PW211604006
    • PW211604009
    • PW211604010
    • PW211605001
    • PW211605002
    • PW211605004
    • PW211605005
    • PW211605006
    • PW211605007
    • PW211606005
    • PW211606007
    • PW211607001
    • PW211607004
    • PW211607005
    • PW211607009
    • PW211607017
    • PW211607018
    • PW211608001
    • PW211608006
    • PW211610002
    • PW211610006
    • PW211610007
    • PW211610008
    • PW211610011
    • PW211611001
    • PW211611002
    • PW211611003
    • PW211611004
    • PW211611005
    • PW211612003
    • PW211612006
    • PW211612007
    • PW211612008
  • Serial numbers OUS

    199 of 199 codes

    • PW201607008
    • PW211409001
    • PW211501001
    • PW211501002
    • PW211501003
    • PW211501004
    • PW211501010
    • PW211501011
    • PW211501012
    • PW211506001
    • PW211506002
    • PW211506003
    • PW211506004
    • PW211506005
    • PW211506006
    • PW211506007
    • PW211507001
    • PW211507002
    • PW211507003
    • PW211507004
    • PW211508001
    • PW211508002
    • PW211508004
    • PW211509001
    • PW211510003
    • PW211511004
    • PW211512002
    • PW211512003
    • PW211601005
    • PW21160113
    • PW21160114
    • PW211602001
    • PW211602005
    • PW211602006
    • PW211603004
    • PW211603005
    • PW211603006
    • PW211604003
    • PW211604004
    • PW211604007
    • PW211604008
    • PW211605008
    • PW211606001
    • PW211606002
    • PW211606003
    • PW211606004
    • PW211606006
    • PW211606008
    • PW211607002
    • PW211607003
    • PW211607006
    • PW211607007
    • PW211607010
    • PW211607011
    • PW211607012
    • PW211607013
    • PW211607014
    • PW211607015
    • PW211607016
    • PW211608002
Amount recalled
291 units

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

Why it was recalled

Potential exposure to biohazard. Software design problem causes excess speed and vibrations in the unload arm movement which causes caused sample splashing.

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

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Mar 11, 2022 · Data as of Sep 19, 5:29 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.