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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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Critical RiskFDA Food
Food & Beverages/Dietary Supplements

White Maeng Da Kratom Powder Recalled for Possible Salmonella

Agency Publication Date: February 5, 2025
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Summary

COREPACK MANUFACTURING INC is recalling approximately 5,520 units of White Maeng Da Kratom Powder due to the potential presence of Salmonella. The product was sold in 3 oz mylar resealable bags and distributed to retailers throughout the United States. No illnesses or injuries have been reported to date in connection with this recall.

Risk

Salmonella is a bacterium that can cause serious and sometimes fatal infections, particularly in young children, the elderly, and those with weakened immune systems. Symptoms of infection include fever, diarrhea (which may be bloody), nausea, vomiting, and abdominal pain.

What You Should Do

  1. The recalled product is White Maeng Da Kratom Powder sold in 3 oz mylar resealable bags, often packed 80 bags per shipper box.
  2. Check your packaging for lot number CP11122. Although not explicitly printed on the label, these products have an expiration date of April 2024.
  3. Return the product to the place of purchase for a refund, throw it away, or contact the manufacturer for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls for additional information.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: White Maeng Da Kratom Powder (3 oz)
Variants: 3 oz package
Lot Numbers:
CP11122 (Exp April 2024)

Expiration date of April 2024 is not included on the label.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 95973
Status: Resolved
Manufacturer: COREPACK MANUFACTURING INC
Sold By: Retailers throughout the United States
Manufactured In: United States
Units Affected: 5520 units
Distributed To: Nationwide
Agency Last Updated: June 20, 2025

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.