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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

Remel Campy CVA Medium Recalled for Low Recovery of Campylobacter Jejuni

Agency Publication Date: February 26, 2026
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Summary

Remel, Inc. is recalling 97 units of its Campy CVA Medium 100/PK laboratory diagnostic plates. The recall was initiated because customer complaints indicated the medium had low to no recovery of Campylobacter Jejuni ATCC 33291. Consumers should stop using the affected medium immediately and contact the manufacturer to arrange for a return or replacement.

Risk

The defect causes the medium to fail to grow the targeted bacteria, which can lead to false-negative results in clinical or diagnostic laboratory testing.

What You Should Do

  1. Identify the affected product by checking the packaging for Campy CVA Medium 100/PK with Catalog Number R01272, Lot 339135, and an expiration date of January 12, 2026.
  2. Stop using the recalled product immediately.
  3. Contact Remel, Inc. or your distributor to arrange for a return, replacement, or correction of the identified lot.
  4. Call the FDA at 1-888-463-6332 (1-888-INFO-FDA) for additional questions regarding 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: Campy CVA Medium 100/PK
Model / REF:
R01272
Lot Numbers:
339135 (Exp January 12, 2026)
UDI:
848838001055

Catalog number R01272 is listed as both the product and lot identifier in source data.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98403
Status: Active
Manufacturer: Remel, Inc
Sold By: Laboratory distributors
Manufactured In: United States
Units Affected: 97
Distributed To: Arizona, Colorado, Illinois, New Jersey, Ohio, Tennessee, Washington

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.