ACTIVE RECALL — CLASS IIActive recallH-1146-2026/FDA enforcement
Wise Foods INC·Food·May 28, 2026

Wise Onion Rings, 3.75 OZ, Metalized Film in Cardboard Cartons, 14 Bags Per Case

What you need to know

Class II
  • What happened

    The product contains undeclared Yellow 5 and 6, Blue 1, and unapproved Red 3.

  • 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 FDANC, VA, PA, NJ +3 moreMore food

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Product identification

Source: FDA FOOD

Brand nameWise Foods INC
Recalling firmWise Foods INCBerwick, PA, United States
UPC / barcodes
0 41262 28887 4
Lot / date codes
  • UPC: 041262288874 Internal production number: 4228887 Lot Codes (expiration date): AUG0326, AUG1026, AUG1726
Distribution area
NCVAPANJNYSCFL

The adulterated product was distributed to the following States: NC, VA, PA, NJ, NY, SC, FL

United States

Quantity affected490 cases
Recall initiationFDA report date: July 15, 2026
FDA recall numberH-1146-2026

Beyond the headline

The recall, in context

Wise Foods INC initiated this food recall on May 28, 2026. The FDA enforcement report states: The product contains undeclared Yellow 5 and 6, Blue 1, and unapproved Red 3. The FDA report lists distribution as: The adulterated product was distributed to the following States: NC, VA, PA, NJ, NY, SC, FL.

The FDA enforcement report describes the reason as: The product contains undeclared Yellow 5 and 6, Blue 1, and unapproved Red 3.

Wise Onion Rings, 3.75 OZ, Metalized Film in Cardboard Cartons, 14 Bags Per Case was made or distributed by Wise Foods INC in Berwick, PA, United States. This page reflects FDA report H-1146-2026, dated July 15, 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 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 Wise Onion Rings, 3.75 OZ, Metalized Film in Cardboard Cartons, 14 Bags Per Case recall?

Wise Foods INC recalled Wise Onion Rings, 3.75 OZ, Metalized Film in Cardboard Cartons, 14 Bags Per Case in an FDA Class II enforcement action reported as H-1146-2026. The product contains undeclared Yellow 5 and 6, Blue 1, and unapproved Red 3.

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 Wise Foods 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 H-1146-2026. 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.