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Lower risk Food recall · FDA · Published October 27, 2020

CELTRADE Pacific Jade Curry Sauce Recall: Wrong Anchovy Ingredient

CELTRADE Canada recalls Pacific Jade Indian Curry Sauce Starter with Fenugreek and Cardamom due to incorrect anchovy ingredient listed on shipping case. This mismatch may cause confusion about product contents.

🇺🇸 FDA recall #F-0139-2021FoodCELTRADE ›
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Recalling firmCELTRADE CANADA7566 Bath Rd · Mississauga, Canada
✎ GovInfoNow plain-language explainer

CELTRADE Canada is recalling Pacific Jade Indian Curry Sauce Starter products because the shipping case lists anchovy as an ingredient, but the actual product does not contain anchovy. This mismatch could lead to confusion about what's in the sauce. Read more at govinfonow.com/recall/15049-celtrade-pacific-jade-curry-sauce-recall-wrong-anchovy-ingredient.

Source Summary by GovInfoNow · govinfonow.com/recall/15049-celtrade-pacific-jade-curry-sauce-recall-wrong-anchovy-ingredient · Updated October 4, 2026 · FDA enforcement record: FDA #F-0139-2021

Cite this page

“CELTRADE Pacific Jade Curry Sauce Recall: Wrong Anchovy Ingredient.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/15049-celtrade-pacific-jade-curry-sauce-recall-wrong-anchovy-ingredient. Based on FDA recall #F-0139-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0139-2021%22&limit=1).

The Food and Drug Administration announced on Oct. 27, 2020, that CELTRADE CANADA is recalling Pacific Jade Indian Curry Sauce Starter because the inner product contains anchovy, an undeclared allergen not listed on the shipping case label.

How to tell if you have it

  • Brand: CELTRADE
  • Product: Pacific Jade Indian Curry Sauce Starter With Fenugreek and Cardamom, wholesale case with 2, 39 oz. plastic tubs
  • UPC: 50758108742487
  • Lot code: 0060220

The hazard

The product declared on the shipping case does not match the inner packaged product. The inner packaged product contains anchovy, which is not an ingredient of the product identified on the shipping case.

Context

GovInfoNow's records show other recent recalls of similar products include Albertsons Wok Pad Thai Chicken Recall: Missing Anchovy Label (2026-05-06), Albertsons Wok Pad Thai Chicken with Egg Roll Recall: Missing Anchovy Label (2026-05-06), and Albertsons Wok Pad Thai Chicken Recall: No Anchovy Declaration (2026-05-06).

How to tell if you have this one

Check for the Pacific Jade Indian Curry Sauce Starter with Fenugreek and Cardamom, wholesale case with 2, 39 oz. plastic tubs, case UPC 50758108742487, batch code 0060220. The product does not contain anchovy, but the shipping case lists it as an ingredient.

  • Brand
    CELTRADE
  • Product
    Pacific Jade Indian Curry Sauce Starter With Fenugreek and Cardamom, wholesale case with 2, 39 oz. plastic tubs, case
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the product name, UPC code 50758108742487, and batch code 0060220 on the shipping case.

Where it went and when

Where it was distributed

Distributed in Illinois.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “IL” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Illinois.

Recall timeline

FDA terminated this recall 34 days after the firm started it.

1. Firm started the recall: Oct 27, 202012. FDA classified it Class II: Nov 30, 202023. FDA terminated the recall: Nov 30, 202034. Published in FDA’s Enforcement Report: Dec 9, 202042020
  1. Firm started the recall
  2. FDA classified it Class II
  3. FDA terminated the recall
  4. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

Is there a risk of injury from this product?

No, this is a labeling error that does not pose a physical risk. The hazard is confusion about ingredients, not a safety hazard.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-0139-2021 (October 27, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0139-2021 to see it in context.
  • Plain-language summary written by qwen3:4b on October 4, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA