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ACTIVE RECALL — CLASS IIIActive recallH-0759-2026/FDA enforcement
Silver Moon Lp Dba Loard's Ice Cream·Food·Apr 15, 2026

Peppermint Ice Cream - 32 OZ (4 Labels: Mollie Stone's

What you need to know

Class III

  • What happened

    Undeclared Red #40

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. 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.

Active recall · classified by the FDAINMore food

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Product identification

Source: FDA FOOD

Brand nameSilver Moon Lp Dba Loard's Ice Cream
Recalling firmSilver Moon Lp Dba Loard's Ice CreamSan Leandro, CA, United States
UPC / barcodes
81201700933
Lot / date codes
  • UPC: 8-12017-00933
Distribution area
IN

Loard's brand distributed to Loard's Ice Cream parlors located in Northern California. Private labels distributed to grocery stores located in Northern California.

United States

Quantity affected1076 TOTAL units (32 oz/unit)
Recall initiationFDA report date: May 13, 2026
FDA recall numberH-0759-2026

Beyond the headline

The recall, in context

Silver Moon Lp Dba Loard's Ice Cream initiated this food recall on April 15, 2026. The FDA enforcement report states: Undeclared Red #40. The FDA report lists distribution as: Loard's brand distributed to Loard's Ice Cream parlors located in Northern California. Private labels distributed to grocery stores located in Northern California.

The FDA enforcement report describes the reason as: Undeclared Red #40

Peppermint Ice Cream - 32 OZ (4 Labels: Mollie Stone's was made or distributed by Silver Moon Lp Dba Loard's Ice Cream in San Leandro, CA, United States. This page reflects FDA report H-0759-2026, dated May 13, 2026.

Why this is a Class III recall

Class III means the product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. 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 is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations.

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 allergen

Symptoms to watch for

Hives, swelling, wheezing, coughing, vomiting, abdominal pain or a drop in blood pressure. Anaphylaxis is a medical emergency.

When symptoms may appear

Allergic reactions often begin within minutes to a few hours of eating the allergen.

Higher-risk groups

Anyone with a diagnosed food allergy, especially children, and people with a history of anaphylaxis or asthma.

What to do now

  1. 1Do not eat or serve the affected product if you or anyone in the household has a diagnosed allergy.
  2. 2If symptoms such as swelling, wheezing or breathing difficulty occur, use the person's prescribed emergency plan and call emergency services.
  3. 3Keep the packaging, contact the retailer or manufacturer for a refund, and read the official recall notice for the exact allergen.

For a severe allergic reaction, do not wait for a callback or refund process before seeking emergency care.

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 Peppermint Ice Cream - 32 OZ (4 Labels: Mollie Stone's recall?

Silver Moon Lp Dba Loard's Ice Cream recalled Peppermint Ice Cream - 32 OZ (4 Labels: Mollie Stone's in an FDA Class III enforcement action reported as H-0759-2026. Undeclared Red #40

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 or serve the affected product if you or anyone in the household has a diagnosed allergy. If symptoms such as swelling, wheezing or breathing difficulty occur, use the person's prescribed emergency plan and call emergency services. Keep the packaging, contact the retailer or manufacturer for a refund, and read the official recall notice for the exact allergen.

Is the Silver Moon Lp Dba Loard's Ice Cream recall still active?

Yes. As of the latest FDA enforcement report, this recall is listed as ongoing. Check the official source record for the most current status before making a decision.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record H-0759-2026. 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 Silver Moon Lp Dba Loard's Ice Cream

View brand
Class II·

Silver Moon Lp Dba Loard's Ice Cream

Loard's Champagne Sherbert - 32 OZ

Undeclared Milk, Red #40.

INFood
Class II·

Silver Moon Lp Dba Loard's Ice Cream

Chocolate Showers Ice Cream - 32 OZ (5 Labels: Mollie Stone's

Undeclared Soy (with mitigating circumstances)

INFood

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