ACTIVE RECALL — CLASS IIActive recallH-0716-2026/FDA enforcement

Loard's Black Raspberry Ice Cream - 32 OZ

What you need to know

Class II
  • What happened

    Undeclared Milk, Red #40, Blue #1.

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. 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 / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codesNo lot code listed. Follow the recall notice and check the packaging.
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 affected446 units (32 oz/unit)
Recall initiationFDA report date: May 13, 2026
FDA recall numberH-0716-2026

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 Milk, Red #40, Blue #1. 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 Milk, Red #40, Blue #1.

Loard's Black Raspberry Ice Cream - 32 OZ 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-0716-2026, dated May 13, 2026.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. 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 may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

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 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 Loard's Black Raspberry Ice Cream - 32 OZ recall?

Silver Moon Lp Dba Loard's Ice Cream recalled Loard's Black Raspberry Ice Cream - 32 OZ in an FDA Class II enforcement action reported as H-0716-2026. Undeclared Milk, Red #40, Blue #1.

What are the symptoms of Undeclared milk exposure?

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with a milk allergy.

How quickly can Undeclared milk symptoms appear?

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

Who is most at risk from Undeclared milk?

People with a diagnosed cow's milk allergy, especially children and anyone with a history of anaphylaxis.

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.

How do I get a refund from Silver Moon Lp Dba Loard's Ice Cream?

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall H-0716-2026 and keep the packaging, lot code and proof of purchase if you have them.

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-0716-2026. 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

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