Mad Batter Bakery Cranberry Orange Scones Recall: Undeclared Allergens
Mad Batter Bakery's Cranberry Orange Scones (5oz) may contain undeclared milk, egg, soy, and wheat. Consumers should avoid these products due to allergy risks.
Lower-risk recall
Cranberry Orange Scones are recalled because they may contain undeclared Milk, Egg, Soy, and Wheat.
Contact the company
What happened, in plain English
Mad Batter Bakery's Cranberry Orange S: 5oz scones may contain undeclared milk, egg, soy, and wheat. This recall affects people with allergies to these ingredients, who could experience allergic reactions. Read more at govinfonow.com/recall/22589-mad-batter-bakery-cranberry-orange-scones-recall-undeclared-allergens.
Source Summary by GovInfoNow · govinfonow.com/recall/22589-mad-batter-bakery-cranberry-orange-scones-recall-undeclared-allergens · Updated October 8, 2026 · FDA enforcement record: FDA #F-1085-2017
Cite this page
“Mad Batter Bakery Cranberry Orange Scones Recall: Undeclared Allergens.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/22589-mad-batter-bakery-cranberry-orange-scones-recall-undeclared-allergens. Based on FDA recall #F-1085-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1085-2017%22&limit=1).
Why it’s dangerous
The scones may contain undeclared allergens that could trigger allergic reactions in sensitive individuals. This is a food safety issue related to ingredient labeling.
Who’s affected
People with milk, egg, soy, or wheat allergies are at risk from consuming these scones. The recall applies to all consumers who purchased the product.
How to tell if you have this one
Check for the product name 'Cranberry Orange Scone' with a 5oz net weight. The packaging includes a plastic film wrapper with labeling on the back of the package.
- Brand
Mad Batter Bakery- Category
Food
What to do — step by step
Check Product Label
Look for the product name 'Cranberry Orange Scone' with a 5oz net weight and plastic film wrapper.
Where it went and when
Where it was distributed
Distributed in Washington.
FDA distribution: “distributed in WA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Washington.
Recall timeline
FDA terminated this recall 29 days after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
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 #F-1085-2017 (December 14, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1085-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 8, 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.