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Ongoing FDAEvent 98857 (5 months ago)

Cafe Nouria Blueberry Muffin

The blueberry muffin contains undeclared walnuts, which can cause serious or life-threatening allergic reactions in people with tree nut allergies.

Moderate risk

Eating it may cause temporary or medically reversible health problems. Serious harm is unlikely.

FDA Class II recall · How risk is rated

2 photos

What to do

What happened

The Brownie Baker Inc. of Fresno, California is voluntarily recalling cafe nouria blueberry muffin NET WT. 6 OZ (170g) because the product contains undeclared walnuts. The recall began April 27, 2026, and was announced by the company on May 7, 2026. The product was distributed in Illinois.

The recalled muffins were incorrectly labeled as blueberry muffins but are Nouria Banana Nut Muffins, which contain walnuts. The recall involves 432 cases, with 9 units per case, totaling 3,888 units. The FDA classified the recall on May 29, 2026, and added it to the Enforcement Report on June 1, 2026.

Summary by Recall Canary from the FDA notice.

What to do

If a code on your package matches:

  1. Consumers who have purchased this product and have a tree nut allergy should not consume the product.
  2. You are urged to check with their place of purchase if unsure whether they have the affected product.
  3. The Brownie Baker recommends that the product be disposed of safely or returned to the place of purchase.
  4. Consumers with questions may contact. The Brownie Baker, Inc.Phone: 559-277-7070Mon-Fri, 8:00 AM-4:00 PM Pacific Time.

Is yours affected?

Match the UPC and lot code listed under your product.

  1. cafe nouria blueberry muffin

    UPC
    • 811070033986
    Lot
    • 6082
  2. Nouria Banana Nut Muffin (labeled as Blueberry Muffin)

    UPC
    • 811070033979
    Lot code
    • 6082
  3. Lot code
    • 6082
Label photo

Details

Company began the recall
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U.S. Distribution: Illinois Foreign Distribution: Not Applicable

Event ID
98857
Recall No.
H-0859-2026
Company
The Brownie Baker Inc.Fresno, California
Quantity recalled
432 cases (9 units/case); 3,888 units
  1. Company began the recall

  2. Announced by the company

  3. Listed on Recall Canary

  4. Classified by FDA

  5. Added to FDA's Enforcement Report

  6. In FDA's weekly enforcement report

  7. Summary updated

Summary by Recall Canary, written with AI · summary updated Oct 7, 2026 · primary source: U.S. Food and Drug Administration