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Lower risk Food recall · FDA · Published June 5, 2017

Western Family Onion Soup Mix Recall: Undeclared Egg Risk

Western Family recalls onion soup mix pouches that may contain undeclared egg. Consumers should check product labels and contact the company for details.

🇺🇸 FDA recall #F-2366-2017FoodWestern Family ›
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Contact the company

Recalling firmGilster-Mary Lee Corp.1037 State St · Chester, IL 62233-1657
✎ GovInfoNow plain-language explainer

What happened, in plain English

Western Family is recalling onion soup mix pouches that may contain undeclared egg. This could pose a risk for people with egg allergies. The recall is for specific packaging and best-by dates. Read more at govinfonow.com/recall/21141-western-family-onion-soup-mix-recall-undeclared-egg-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/21141-western-family-onion-soup-mix-recall-undeclared-egg-risk · Updated October 8, 2026 · FDA enforcement record: FDA #F-2366-2017

Cite this page

“Western Family Onion Soup Mix Recall: Undeclared Egg Risk.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/21141-western-family-onion-soup-mix-recall-undeclared-egg-risk. Based on FDA recall #F-2366-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2366-2017%22&limit=1).

Why it’s dangerous

The soup mix may contain egg that wasn't listed on the label. This could cause allergic reactions in people who are sensitive to egg. The risk is only for those with known egg allergies.

Who’s affected

People with egg allergies are most at risk from this recall. The product is sold in pouches packaged in cartons with specific best-by dates.

How to tell if you have this one

Check for Western Family Onion Soup Mix pouches in 4.5-oz cartons with a Best By date of APR 10 18 D16. The product has a UPC code of 15400-03604.

  • Brand
    Western Family
  • Product
    Western Family Onion Soup Mix, 2.25 oz. pouches packaged in 4.5-oz. cartons
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the product name and UPC code on the packaging to confirm it's the recalled item.

Where it went and when

Where it was distributed

Distributed in Utah.

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: yesUTColorado: 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: “Domestic only: ASSOCIATED FOODS STORES FARR WEST WAREHOUSE 1850 WEST 2530 NORTH FARR WEST, UT 84404” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Utah.

Recall timeline

FDA terminated this recall 3 months after the firm started it.

1. Firm started the recall: Jun 5, 201712. FDA classified it Class I: Jun 9, 201723. Published in FDA’s Enforcement Report: Jun 21, 201734. FDA terminated the recall: Aug 25, 201742017
  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.

✎ GovInfoNow

Questions people ask

What should I do if I have this product?

The recall does not require immediate action, but you should check the product label and contact Western Family if you have concerns.

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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-2366-2017 (June 5, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2366-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 8, 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