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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 Multidrug Resistant MIC 1 Panels Recalled for Manufacturing Issue

Agency Publication Date: April 8, 2026
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Summary

Beckman Coulter, Inc. is recalling 3 boxes of MicroScan Neg Multidrug Resistant MIC 1 panels due to a manufacturing issue where the tests were processed incorrectly. These panels are used in laboratory settings to identify bacteria and determine which antimicrobial drugs will be effective against them. No injuries or incidents have been reported, but incorrect processing could lead to inaccurate test results used for treating infections.

Risk

A manufacturing error caused these diagnostic panels to be processed incorrectly, which may result in laboratory errors when identifying multidrug-resistant bacteria or determining their drug susceptibility. This could potentially lead to a patient receiving the wrong antibiotic treatment.

What You Should Do

  1. Identify the affected product by looking for MicroScan Neg Multidrug Resistant MIC 1 panels with Catalog Number C32368, Lot Number 2026-05-08, and UDI-DI code 15099590720568.
  2. Stop using the recalled product immediately.
  3. Contact the manufacturer, Beckman Coulter, Inc., or your distributor to arrange for a return, replacement, or correction of the affected units.
  4. For additional questions or to report issues, call the FDA at 1-888-463-6332 (1-888-INFO-FDA).

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 Multidrug Resistant MIC 1 (3 boxes)
Model / REF:
C32368
Lot Numbers:
2026-05-08
UDI:
15099590720568

Intended for use with MicroScan Dried Gram Negative MIC/Combo Panels.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98562
Status: Active
Manufacturer: Beckman Coulter, Inc.
Sold By: Direct distribution
Manufactured In: United States
Units Affected: 3 boxes

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.