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Serious recall: Injury is possible or has been reported. Take action promptly.

Beckman Coulter Inc. 2026-08-12 Health serious FDA
Health · FDA · Recall #FDA-Z-2889-2026

REF # D23354, MicroScan LabPro V5.03 Panel Update 11 DVD Kit (US) on the following… Recall

Issued August 12, 2026 · Beckman Coulter Inc.

In August 2026, Beckman Coulter Inc. recalled the REF # D23354, MicroScan LabPro V5.03 Panel Update 11 DVD Kit (US) on the following…, a serious health recall reported by the FDA.

Compiled by Dana Whitfield, RecallCheckr

What this means for you

Analyzers contain incorrect algorithms which may affect antimicrobial susceptibility test results, leading to false susceptibility classifications."

What you should do

  1. 1 Stop using REF # D23354, MicroScan LabPro V5.03 Panel Update 11 DVD Kit (US) on the following… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Beckman Coulter Inc. to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
Beckman Coulter Inc.
Category
Health
Recall date
August 12, 2026
Units affected
Not reported
Sold at
US Nationwide distribution including in the states of AK, AL, AR, CA, CO, DE, FL, GA, IA, IL, IN, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, ND
Recall number
FDA-Z-2889-2026
Made in
United States
Issuing agency
FDA

In context

  • Beckman Coulter Inc. has 5 recalls in our database.
  • We're tracking 3,707 Health recalls in our database.
  • This is the 487th Health recall we've logged in 2026.
Read the official FDA notice

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