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ACTIVE RECALL — CLASS IActive recallF-0621-2017/FDA enforcement
Commerce International INC.·Food·Aug 5, 2016

Eastern Feast, Green Raisin, 7 OZ, 11 OZ, and 14 OZ Plastic Containers

What you need to know

Class I

  • What happened

    Initiated by the Florida Department of Agriculture and Consumer Services due to undeclared sulfites on the finished product label.

  • 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.

Active recall · classified by the FDAFL, GA, NC, SCMore food

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameCommerce International INC.
Recalling firmCommerce International INC.Orlando, FL, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • No lot codes
Distribution area
FLGANCSC

FL, GA, NC, and SC.

United States

Quantity affectedAt least approximately 688.5 pounds
Recall initiationFDA report date: December 14, 2016
FDA recall numberF-0621-2017

Beyond the headline

The recall, in context

Commerce International INC. initiated this food recall on August 5, 2016. The FDA enforcement report states: Initiated by the Florida Department of Agriculture and Consumer Services due to undeclared sulfites on the finished product label. The FDA report lists distribution as: FL, GA, NC, and SC.

The FDA enforcement report describes the reason as: Initiated by the Florida Department of Agriculture and Consumer Services due to undeclared sulfites on the finished product label.

Eastern Feast, Green Raisin, 7 OZ, 11 OZ, and 14 OZ Plastic Containers was made or distributed by Commerce International INC. in Orlando, FL, United States. This page reflects FDA report F-0621-2017, dated December 14, 2016.

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 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 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 Eastern Feast, Green Raisin, 7 OZ, 11 OZ, and 14 OZ Plastic Containers recall?

Commerce International INC. recalled Eastern Feast, Green Raisin, 7 OZ, 11 OZ, and 14 OZ Plastic Containers in an FDA Class I enforcement action reported as F-0621-2017. Initiated by the Florida Department of Agriculture and Consumer Services due to undeclared sulfites on the finished product label.

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 Commerce International INC. 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 F-0621-2017. 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 Commerce International INC.

View brand
Class I·

Commerce International INC.

Eastern Feast, Green Raisin, 7 OZ Plastic Container

Initiated by the Florida Department of Agriculture and Consumer Services due to undeclared sulfites on the finished product label.

Distribution not listedFood

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