RECALL RECORD — CLASS IIIRecall closedF-1064-2022/FDA enforcement

Milk & Dark Chocolate Caramel Macchiato

What you need to know

Class III
  • What happened

    Undeclared Soy Lecithin. Firm used Canola Oil spray as a releasing agent but finished products labels do not declare Soy Lecithin.

  • 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.

Recall closed · classified by the FDAINMore food

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Product identification

Source: FDA FOOD

Brand nameR & S Roberts Enterprises, INC.
Recalling firmR & S Roberts Enterprises, INC.Auburn, WA, United States
UPC / barcodes
7 82565 11777 4
Lot / date codes
  • Manufacture date: 03/22/2022 Tracking By Manufacture Date: 03/22/2022
Distribution area
IN

Distributed in Washington.

United States

Quantity affected48 pieces
Recall initiationFDA report date: May 25, 2022
FDA recall numberF-1064-2022

Beyond the headline

The recall, in context

R & S Roberts Enterprises, INC. initiated this food recall on April 27, 2022. The FDA enforcement report states: Undeclared Soy Lecithin. Firm used Canola Oil spray as a releasing agent but finished products labels do not declare Soy Lecithin. The FDA report lists distribution as: Distributed in Washington.

The FDA enforcement report describes the reason as: Undeclared Soy Lecithin. Firm used Canola Oil spray as a releasing agent but finished products labels do not declare Soy Lecithin.

Milk & Dark Chocolate Caramel Macchiato was made or distributed by R & S Roberts Enterprises, INC. in Auburn, WA, United States. This page reflects FDA report F-1064-2022, dated May 25, 2022.

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 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 Milk & Dark Chocolate Caramel Macchiato recall?

R & S Roberts Enterprises, INC. recalled Milk & Dark Chocolate Caramel Macchiato in an FDA Class III enforcement action reported as F-1064-2022. Undeclared Soy Lecithin. Firm used Canola Oil spray as a releasing agent but finished products labels do not declare Soy Lecithin.

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 R & S Roberts Enterprises, 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 F-1064-2022. 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 R & S Roberts Enterprises, 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.