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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

Pacific Jade Indian Curry Sauce Starter Recalled for Undeclared Anchovy

Agency Publication Date: November 30, 2020
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Summary

Celtrade Canada is recalling 153 cases of Pacific Jade Indian Curry Sauce Starter With Fenugreek and Cardamom because the shipping cases contain a different product than what is printed on the label. The inner packaged product contains anchovy, which is not listed as an ingredient on the outer case label. This recall affects wholesale cases containing two 39 oz. plastic tubs distributed in Illinois.

Risk

People with an allergy or severe sensitivity to anchovy (fish) run the risk of a serious or life-threatening allergic reaction if they consume this product.

What You Should Do

  1. Identify if you have the recalled product by checking for Pacific Jade Indian Curry Sauce Starter With Fenugreek and Cardamom in wholesale cases containing two 39 oz. plastic tubs.
  2. Check the shipping case for UPC 50758108742487 and the batch or lot code 0060220.
  3. Return the product to the place of purchase for a full refund, throw it away, or contact Celtrade Canada for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) 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: Pacific Jade Indian Curry Sauce Starter With Fenugreek and Cardamom (39 oz.)
Variants: Wholesale case with 2, 39 oz. plastic tubs
UPC Codes:
50758108742487
Lot Numbers:
0060220
GTIN:
50758108742487

Recall number F-0139-2021. The inner packaged product does not match the shipping case declaration.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 86676
Status: Resolved
Manufacturer: CELTRADE CANADA
Sold By: Wholesale
Manufactured In: Canada
Units Affected: 153 cases
Distributed To: Illinois

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.