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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 Vet
Pets & Animals/Pet Medications

NeuroLogica Corporation: PT Electrolyte Test 3V Recalled for Inaccurate Sodium and Chloride Results

Agency Publication Date: June 6, 2018
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Summary

NeuroLogica Corporation is recalling 4,940 units of the PT Electrolyte Test 3V, a veterinary diagnostic cartridge. Samsung, the manufacturer, found that a polymer used in the test's reagent was over-oxidized, causing the chemical stability of the sodium and chloride tests to fail. This defect causes the test to produce results that are on the lower end of the acceptable range, which could lead to incorrect medical assessments for animals. These cartridges were distributed nationwide in the United States between 2017 and 2018.

Risk

The oxidized reagent causes inaccurate measurement of sodium and chloride levels in animal blood samples. These stabilized lower-range readings may lead veterinarians to misdiagnose an animal's electrolyte balance, potentially resulting in inappropriate or harmful medical treatments.

What You Should Do

  1. Identify your supply of PT Electrolyte Test 3V cartridges and check for the following lot numbers and expiration dates: Lot# 302QAHAA (Exp. 07/10), Lot# 302QAHB8 (Exp. 08/08), Lot# 302QAHB9 (Exp. 08/09), Lot# 302QAJ1O (Exp. 10/24), Lot# 302QAJ21 (Exp. 11/01), and Lot# 302QAJ22 (Exp. 11/02).
  2. Immediately stop using any electrolyte test cartridges that match the affected lot numbers listed above.
  3. Contact your veterinarian or the clinic's equipment manager to determine if recent test results for sodium or chloride may have been impacted by these specific lots.
  4. Contact the manufacturer, NeuroLogica Corporation, at their Danvers, Massachusetts facility or via their customer support channels to discuss return or replacement options for the affected cartridges.
  5. For additional questions or to report issues, contact the FDA's Center for Veterinary Medicine at 240-402-7002.

Your Remedy Options

๐Ÿ“‹Other Action

Manufacturer initiated contact via letter

How to: Contact your healthcare provider or the manufacturer for further instructions and potential refund

Affected Products

Product: PT Electrolyte Test 3V
Model:
V-0096-2018
Lot Numbers:
302QAHAA (Exp. 07/10)
302QAHB8 (Exp. 08/08)
302QAHB9 (Exp. 08/09)
302QAJ1O (Exp. 10/24)
302QAJ21 (Exp. 11/01)
302QAJ22 (Exp. 11/02)
Date Ranges: Expiration 07/10, Expiration 08/08, Expiration 08/09, Expiration 10/24, Expiration 11/01, Expiration 11/02

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 79022
Status: Resolved
Manufacturer: NeuroLogica Corporation
Manufactured In: United States
Units Affected: 4940 cartridges (units)
Distributed To: Nationwide

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