Brownie Baker Cafe Nouria Blueberry Muffin Recall: Undeclared Walnuts
Brownie Baker recalls cafe nouria blueberry muffins with undeclared walnuts. Consumers should check UPC 811070033986 and lot 6082 for affected products.
Lower-risk recall
Undeclared walnuts
Contact the company
What happened, in plain English
Brownie Baker is recalling blueberry muffins that contain undeclared walnuts. This poses a risk for people with nut allergies who may react to the walnuts. Read more at govinfonow.com/recall/6430-brownie-baker-cafe-nouria-blueberry-muffin-recall-undeclared-walnuts.
Source Summary by GovInfoNow · govinfonow.com/recall/6430-brownie-baker-cafe-nouria-blueberry-muffin-recall-undeclared-walnuts · Updated August 10, 2026 · Official notice: FDA #H-0859-2026
Cite this page
“Brownie Baker Cafe Nouria Blueberry Muffin Recall: Undeclared Walnuts.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/6430-brownie-baker-cafe-nouria-blueberry-muffin-recall-undeclared-walnuts. Based on FDA recall #H-0859-2026.
Why it’s dangerous
The muffins contain walnuts that were not listed on the label. This can cause allergic reactions in people who are sensitive to nuts.
Who’s affected
People with nut allergies are at risk from this recall. The product is sold in the U.S. and may be found in grocery stores.
How to tell if you have this one
Check for the UPC 811070033986 and lot number 6082 on the product packaging. The product is a blueberry muffin with a net weight of 6 ounces.
- Brand
Brownie Baker- Product
cafe nouria blueberry muffin NET WT. 6 OZ (170g) UPC: 811070033986- Category
Food
What to do — step by step
Check Product Label
Look for the UPC 811070033986 and lot number 6082 on the muffin packaging.
Where it went and when
Where it was distributed
Distributed in Illinois, and outside the U.S.
FDA distribution: “U.S. Distribution: IL Foreign Distribution: Not Applicable” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Illinois.
Recall timeline
FDA published this recall 44 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #H-0859-2026 (April 27, 2026)
- Plain-language summary written by qwen3:4b on August 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.