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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

Medica Capillary Tubes Recalled for False Potassium Results

Agency Publication Date: February 13, 2026
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Summary

Medica Corporation is recalling 1,578 units of its Medica Capillary Tubes and EasyBloodGas/EasyStat Capillary Tube Kits. These tubes were found to have a systematic positive bias of up to 20% across the reportable potassium range. This defect can lead to falsely elevated potassium results in patient blood samples. Consumers and laboratory professionals should stop using the affected kits immediately and contact the manufacturer for further instructions.

Risk

The defect causes patient blood samples to show potassium levels that are higher than they actually are. In a clinical setting, false elevation of potassium results could lead to inappropriate medical treatments or a failure to diagnose underlying conditions, potentially causing patient harm.

What You Should Do

  1. Stop using the recalled Medica Capillary Tubes or EasyBloodGas/EasyStat Capillary Tube Kits immediately.
  2. Identify affected products by checking for Model Number 7303, UDI-DI 00840095607575, and Lot Number 25XXX.
  3. Contact Medica Corporation or your distributor to arrange for a return, replacement, or correction of the affected tubes.
  4. Call the FDA at 1-888-463-6332 (1-888-INFO-FDA) or visit www.fda.gov/medical-devices/medical-device-recalls for additional questions.

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: Medica Capillary Tubes; EasyBloodGas/EasyStat Capillary Tube Kit
Model / REF:
7303
Lot Numbers:
25XXX
UDI:
00840095607575

A systematic positive bias of up to 20% identified across the reportable potassium range.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98315
Status: Active
Manufacturer: Medica Corporation
Sold By: Distributors in Russia; Bulgaria; Kazakhstan; Ukraine; Pakistan; Belarus
Manufactured In: United States
Units Affected: 1,578 units

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.