RECALL RECORD — CLASS IIIRecall closedF-0486-2018/FDA enforcement

Premio Strawberry Pralinati, Strawberry with Cocoa, 3.53oz, 10 Units Per Case, Packed in Paper…

What you need to know

Class III
  • What happened

    Gourmet International Inc. is initiating a voluntary recall of cookie products due to undeclared colors.

  • 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 FDAVA, KY, TX, WI +9 moreMore food

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Product identification

Source: FDA FOOD

Brand nameGourmet International INC.
Recalling firmGourmet International INC.Grand Rapids, MI, United States
UPC / barcodes
8 16240 02015 5
Lot / date codes
  • UPC- 8-16240-02015-5 all lots, all dates, all packages
Distribution area
VAKYTXWIDCPAMOFLOHSCALCAIN

Domestic: Domestic only, no VA/DOD KY, TX, WI, Washington DC, PA, VA, MO, FL, OH, SC, AL, CA, IN,

United States

Quantity affected24, 179 cases 241, 790 units
Recall initiationFDA report date: December 20, 2017
FDA recall numberF-0486-2018

Beyond the headline

The recall, in context

Gourmet International INC. initiated this food recall on November 2, 2017. The FDA enforcement report states: Gourmet International Inc. is initiating a voluntary recall of cookie products due to undeclared colors. The FDA report lists distribution as: Domestic: Domestic only, no VA/DOD KY, TX, WI, Washington DC, PA, VA, MO, FL, OH, SC, AL, CA, IN,.

The FDA enforcement report describes the reason as: Gourmet International Inc. is initiating a voluntary recall of cookie products due to undeclared colors.

Premio Strawberry Pralinati, Strawberry with Cocoa, 3.53oz, 10 Units Per Case, Packed in Paper… was made or distributed by Gourmet International INC. in Grand Rapids, MI, United States. This page reflects FDA report F-0486-2018, dated December 20, 2017.

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 Premio Strawberry Pralinati, Strawberry with Cocoa, 3.53oz, 10 Units Per Case, Packed in Paper… recall?

Gourmet International INC. recalled Premio Strawberry Pralinati, Strawberry with Cocoa, 3.53oz, 10 Units Per Case, Packed in Paper… in an FDA Class III enforcement action reported as F-0486-2018. Gourmet International Inc. is initiating a voluntary recall of cookie products due to undeclared colors.

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 Gourmet International 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-0486-2018. 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 Gourmet International INC.

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Related alerts

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