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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Diagnostic Equipment

MicroScan Neg MIC 56 Panels Recalled for Potential Contamination

Agency Publication Date: March 20, 2026
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Summary

Beckman Coulter, Inc. is recalling 685 boxes of MicroScan Neg MIC 56 (REF C42464) laboratory panels due to the likely presence of contamination in the wells. These panels are used in clinical laboratories to identify specific bacteria and determine which antibiotics will be effective against them. Because the wells may be contaminated, the test results could be inaccurate, potentially leading to incorrect treatment decisions for patients.

Risk

Contamination in the test wells can interfere with the identification of bacteria or susceptibility testing, which may result in a patient receiving the wrong antibiotic or an incorrect diagnosis of a bacterial infection.

What You Should Do

  1. Identify if you have the affected product by checking the packaging for Catalog Number C42464 and Lot Number 2026-01-03.
  2. Stop using the recalled product immediately to prevent inaccurate laboratory results.
  3. Contact the manufacturer, Beckman Coulter, Inc., or your distributor to arrange for a return, replacement, or correction of the affected panels.
  4. Call the FDA at 1-888-463-6332 (1-888-INFO-FDA) if you have additional questions or need to report issues related to this recall.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled product. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: MicroScan Neg MIC 56 REF C42464
Model / REF:
C42464
Lot Numbers:
2026-01-03
UDI:
15099590731212

MicroScan panels are designed for use in determining antimicrobial agent susceptibility and/or identification to the species level of aerobic and facultatively anaerobic gram-negative bacilli.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98555
Status: Active
Manufacturer: Beckman Coulter, Inc.
Sold By: Direct from manufacturer; Laboratory distributors
Manufactured In: United States
Units Affected: 685 boxes
Distributed To: California, Colorado, Indiana, Massachusetts, Maryland, Minnesota, Missouri, North Carolina, New Jersey, Oklahoma, Pennsylvania, Texas

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.