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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 Food
Food & Beverages/Packaged & Processed

Every Plate Green Curry Paste Recalled for Potential Spoilage

Agency Publication Date: August 22, 2023
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Summary

Every Plate has recalled 12 units of its one-ounce (28g) Green Curry Paste packets that were included in specific meal kits. The product was exposed to improper temperatures during distribution, leading to potential spoilage and making it unsafe to eat. No illnesses or injuries have been reported to date in connection with this recall. Consumers should return the paste to the place of purchase for a refund or discard it immediately.

Risk

Temperature abuse can lead to the growth of spoilage organisms and harmful bacteria in food products. Consuming spoiled curry paste may cause foodborne illness or digestive distress.

What You Should Do

  1. This recall affects Every Plate Green Curry Paste (one ounce / 28g) packets contained in meal kits identified by meal codes 87 and 116.
  2. Return the product to the place of purchase for a full refund, throw it away, or contact Every Plate directly for further instructions.
  3. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls for 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: Every Plate Green Curry Paste (1 oz / 28g)
Lot Numbers:
Meal code 87
Meal code 116

Recall number F-1460-2023. The product is a small packet contained within a meal kit.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 92768
Status: Resolved
Manufacturer: EVERY PLATE
Sold By: Every Plate
Manufactured In: United States
Units Affected: 12
Distributed To: South Carolina, Arkansas, Illinois, New Mexico, Tennessee, District of Columbia, New Jersey, Virginia

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.