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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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Low RiskFDA Food
Food & Beverages/Produce & Fresh

Madame Sarah Djon Djon Dried Mushrooms Recalled for Undeclared Sulfites

Agency Publication Date: January 8, 2020
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Summary

Horizon Vert Pure Llc is recalling approximately 500 units of Madame Sarah brand Djon Djon dried mushrooms because they contain undeclared sulfites. The recalled mushrooms were distributed in Florida in 1.76oz (50g) packages. Consumers who have purchased this product should return it to the place of purchase for a full refund.

Risk

People who have a severe sensitivity to sulfites run the risk of serious or life-threatening allergic reactions if they consume this product.

What You Should Do

  1. Identify the product by checking for 'MADAME SARAH brand DJON DJON dried mushrooms' in 1.76oz (50g) clear plastic packages with UPC 8 54254 00724 3.
  2. Check the packaging for the distributor statement: 'DISTRIBUTED BY: HORIZON VERT PURE, LLC'. All products within their expiry date are affected.
  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) if you have additional questions.

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: Madame Sarah Djon Djon dried mushrooms (1.76oz / 50g)
UPC Codes:
854254007243
Lot Numbers:
all product within expiry

Product of Haiti; Ingredients listed as Dried Djon Djon Mushrooms; Recall number F-0466-2020.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 84563
Status: Resolved
Manufacturer: Horizon Vert Pure Llc
Sold By: Retailers in Florida
Manufactured In: Haiti, United States
Units Affected: 500 units
Distributed To: Florida

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.