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RECALL RECORD — CLASS IRecall closedF-2366-2017/FDA enforcement
Gilster-mary Lee Corp.·Food·Jun 5, 2017

Western Family Onion Soup Mix, 2.25 OZ

What you need to know

Class I

  • What happened

    The product may contain undeclared egg.

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. An allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

  • Action required

    Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction.

Recall closed · classified by the FDAUTMore food

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Product identification

Source: FDA FOOD

Brand nameGilster-mary Lee Corp.
Recalling firmGilster-mary Lee Corp.Chester, IL, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Western Family Onion Soup Mix, UPC 15400-03604, 2.25 oz. pouches packaged in 4.5-oz. cartons which have a Best By date of APR 10 18 D16
Distribution area
UT

Domestic only: ASSOCIATED FOODS STORES FARR WEST WAREHOUSE 1850 WEST 2530 NORTH FARR WEST, UT 84404

United States

Quantity affected54 cases
Recall initiationFDA report date: June 21, 2017
FDA recall numberF-2366-2017

Beyond the headline

The recall, in context

Gilster-mary Lee Corp. initiated this food recall on June 5, 2017. The FDA enforcement report states: The product may contain undeclared egg. The FDA report lists distribution as: Domestic only: ASSOCIATED FOODS STORES FARR WEST WAREHOUSE 1850 WEST 2530 NORTH FARR WEST, UT 84404.

The FDA enforcement report describes the reason as: The product may contain undeclared egg.

Western Family Onion Soup Mix, 2.25 OZ was made or distributed by Gilster-mary Lee Corp. in Chester, IL, United States. This page reflects FDA report F-2366-2017, dated June 21, 2017.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. In this recall, an allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

FDA definition

The product has a reasonable probability of causing serious adverse health consequences or death.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Undeclared egg

Symptoms to watch for

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with an egg allergy.

When symptoms may appear

Reactions can begin within minutes to a few hours after eating the product.

Higher-risk groups

People with a diagnosed egg allergy, especially children and anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have an egg allergy.
  2. 2Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Western Family Onion Soup Mix, 2.25 OZ recall?

Gilster-mary Lee Corp. recalled Western Family Onion Soup Mix, 2.25 OZ in an FDA Class I enforcement action reported as F-2366-2017. The product may contain undeclared egg.

What should I do if I bought this product?

Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction. Do not eat the product if you have an egg allergy. Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis. Keep the packaging and contact the retailer or manufacturer about a refund.

Is the Gilster-mary Lee Corp. recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-2366-2017. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.