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Stop using now Food recall · FDA · Published November 17, 2021

WEL-PAC Shrimp Dashi Recall: Undeclared Fish Allergen

JFC International recalls WEL-PAC Shrimp Dashi No Moto due to undeclared fish allergens. Check your pantry for this powdered shrimp stock.

🇺🇸 FDA recall #F-0231-2022FoodWEL-PAC ›
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Contact the company

Recalling firmJ F C International Inc7101 E Slauson Ave · Commerce, CA 90040-3622
✎ GovInfoNow plain-language explainer

J F C International Inc is recalling WEL-PAC Brand Shrimp Dashi No Moto because the label failed to declare fish ingredients. The product contains hydrolyzed protein derived from bonito, sardine, and tuna, which are not listed on the packaging. This poses a risk to individuals with fish allergies who may unknowingly consume the allergen. Read more at govinfonow.com/recall/13725-wel-pac-shrimp-dashi-recall-undeclared-fish-allergen.

Source Summary by GovInfoNow · govinfonow.com/recall/13725-wel-pac-shrimp-dashi-recall-undeclared-fish-allergen · Updated October 10, 2026 · FDA enforcement record: FDA #F-0231-2022

Cite this page

“WEL-PAC Shrimp Dashi Recall: Undeclared Fish Allergen.” GovInfoNow, updated October 10, 2026. https://govinfonow.com/recall/13725-wel-pac-shrimp-dashi-recall-undeclared-fish-allergen. Based on FDA recall #F-0231-2022 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0231-2022%22&limit=1).

The FDA announced on November 17, 2021, that J F C International Inc is recalling WEL-PAC Brand Shrimp Dashi No Moto Powdered Stock because the label fails to declare fish allergens. The agency said the undeclared hydrolyzed protein contains bonito, sardine, and tuna.

How to tell if you have it

  • WEL-PAC Brand Shrimp Dashi No Moto - Powdered Shrimp Stock; Net Wt. 1.75 oz. (0.35.oz x 5 bags) 49.6 g UPC: 0 11152
  • UPC: 00011152836607

The hazard

The manufacturer notified the U.S. supplier that the powdered shrimp stock did not declare fish (hydrolyzed protein that contains bonito, sardine and tuna) on the label.

Context

GovInfoNow's records show J F C International Inc has 8 other recalls on record since October 14, 2014. Other recent recalls of similar products include Pack'n Fresh Hondashi Seasoning Recall (July 9, 2026), Eunha Fisheries FLOUNDER SASHIMI With Undeclared Allergens - Recall (July 1, 2026) and Gellert Global Group Kimbap Recall: Undeclared Fish Allergen Risk (June 25, 2026).

How to tell if you have this one

Look for WEL-PAC Brand Shrimp Dashi No Moto - Powdered Shrimp Stock in 1.75 oz packages (containing five 0.35 oz bags). The net weight is 49.6 g and the UPC is 0 11152 83660 7. The product was distributed exclusively in Hawaii.

  • Brand
    WEL-PAC
  • Product
    WEL-PAC Brand Shrimp Dashi No Moto - Powdered Shrimp Stock; Net Wt. 1.75 oz. (0.35.oz x 5 bags) 49.6 g UPC: 0 11152
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Stop consuming the product

    Do not eat the recalled shrimp stock if you have a fish allergy or wish to avoid undeclared ingredients.

  2. Check your pantry

    Verify if you have the specific WEL-PAC product with UPC 0 11152 83660 7 distributed in Hawaii.

Where it went and when

Where it was distributed

Distributed in Hawaii.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: 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: yesHITexas: not listedTXFlorida: not listedFL

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

States: Hawaii.

Recall timeline

FDA terminated this recall 51 days after the firm started it.

1. Firm started the recall: Nov 17, 202112. FDA classified it Class I: Dec 2, 202123. Published in FDA’s Enforcement Report: Dec 8, 202134. FDA terminated the recall: Jan 7, 2022420212022
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

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

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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-0231-2022 (November 17, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0231-2022 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 10, 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