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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 CAMHB and Brucella Broth Recalled for Media Contamination

Agency Publication Date: November 21, 2025
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Summary

Remel, Inc. is recalling CAMHB W/LHB (Manual, 11ml) and Brucella Broth (11ml) because these products may contain contamination. This contamination can cause the laboratory media to turn a darker or brown color, making it unusable or potentially leading to incorrect test results. Approximately 1,000 units in the US and 280 units in the rest of the world are affected by this voluntary recall. Laboratory professionals should immediately stop using these specific lots and contact the manufacturer or their distributor for a replacement or return.

Risk

The contamination of the growth media can interfere with laboratory testing, potentially resulting in inaccurate diagnostic data or the inability to interpret test results. No injuries or incidents have been reported to date.

What You Should Do

  1. This recall involves Remel CAMHB W/LHB manual 11ml media (Product YCP112-10) and Brucella Broth 11ml (Product YT3450) used for laboratory testing.
  2. Identify affected CAMHB products by checking for UDI-DI 848838018831 and lot numbers 305529, 311228, 316019, or 320993.
  3. Identify affected Brucella Broth by checking for UDI-DI 848838091353 and lot number 317287.
  4. Stop using the recalled product. Contact the manufacturer or your distributor to arrange return, replacement, or correction.
  5. Call the FDA: 1-888-463-6332 (1-888-INFO-FDA) for additional information regarding medical device recalls.

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: CAMHB W/LHB, MANUAL, 11ML, 10/BOX
Variants: 11ml, 10/Box
Model / REF:
YCP112-10
Lot Numbers:
305529
311228
316019
320993
UDI:
848838018831

Media may contain contamination resulting in darker or brown color.

Product: BRUCELLA BROTH, 11ML, 10/BOX
Variants: 11ml, 10/Box
Model / REF:
YT3450
Lot Numbers:
317287
UDI:
848838091353

Media may contain contamination resulting in darker or brown color.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97967
Status: Active
Manufacturer: Remel, Inc
Sold By: Laboratory distributors
Manufactured In: United States
Units Affected: 1,000 US, 280 ROW
Distributed To: Alaska, California, Florida, Georgia, Iowa, Illinois, Indiana, Louisiana, Massachusetts, Maryland, Maine, Michigan, Minnesota, Nebraska, New York, Ohio, Oklahoma, Pennsylvania, Rhode Island, South Dakota, Tennessee, Virginia, Washington, Wisconsin

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.