RECALL RECORD — CLASS IRecall closedH-0348-2025/FDA enforcement
Jalux America INC·Food·Jul 10, 2025

Lespoir Cookie, NET Weight: 1.41 OZ

What you need to know

Class I
  • What happened

    Undeclared Milk

  • 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 FDACA, IL, WAMore food

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Product identification

Source: FDA FOOD

Brand nameJalux America INC
Recalling firmJalux America INCEl Segundo, CA, United States
UPC / barcodes
4 942737 20014 7
Lot / date codes
  • Best Before date: September 26, 2025
Distribution area
CAILWA

CA, IL, WA

United States

Quantity affected32 units
Recall initiationFDA report date: August 6, 2025
FDA recall numberH-0348-2025

Beyond the headline

The recall, in context

Jalux America INC initiated this food recall on July 10, 2025. The FDA enforcement report states: Undeclared Milk. The FDA report lists distribution as: CA, IL, WA.

The FDA enforcement report describes the reason as: Undeclared Milk

Lespoir Cookie, NET Weight: 1.41 OZ was made or distributed by Jalux America INC in El Segundo, CA, United States. This page reflects FDA report H-0348-2025, dated August 6, 2025.

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 UPC and lot code 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 milk

Symptoms to watch for

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with a milk 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 cow's milk allergy, especially children and anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a milk 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 Lespoir Cookie, NET Weight: 1.41 OZ recall?

Jalux America INC recalled Lespoir Cookie, NET Weight: 1.41 OZ in an FDA Class I enforcement action reported as H-0348-2025. Undeclared Milk

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 a milk 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 Jalux America INC 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 H-0348-2025. 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

Brand history

More recalls by Jalux America INC

View brand

Related alerts

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