Dannon Dairy Drink Nut & Cereal Bottles Recall: Incorrect Allergen Labeling
Dannon recalls 7.7 fl oz dairy drink nut and cereal bottles due to incorrect allergen labeling. The product lists 'walnut' but contains pecan instead. Consumers should check UPC 36632 01421 and expiration dates.
Lower-risk recall
The label incorrectly states "WALNUT" in the ingredient list and the allergen statement, while the product actually contains PECAN as an ingredient.
Contact the company
What happened, in plain English
Dannon is recalling certain dairy drink nut and cereal bottles because the label incorrectly states 'walnut' as an ingredient when it actually contains pecan. This could cause allergic reactions for people sensitive to pecan. Read more at govinfonow.com/recall/22461-dannon-dairy-drink-nut-cereal-bottles-recall-incorrect-allergen-labeling.
Source Summary by GovInfoNow · govinfonow.com/recall/22461-dannon-dairy-drink-nut-cereal-bottles-recall-incorrect-allergen-labeling · Updated October 8, 2026 · FDA enforcement record: FDA #F-1440-2017
Cite this page
“Dannon Dairy Drink Nut & Cereal Bottles Recall: Incorrect Allergen Labeling.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/22461-dannon-dairy-drink-nut-cereal-bottles-recall-incorrect-allergen-labeling. Based on FDA recall #F-1440-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1440-2017%22&limit=1).
Why it’s dangerous
The product label incorrectly lists 'walnut' as an allergen, but the actual ingredient is pecan. This could lead to allergic reactions in individuals sensitive to pecan.
Who’s affected
People who own or consume the recalled Dannon Dairy Drink Nut & Cereal bottles with UPC 36632 01421. Those with pecan allergies are at higher risk.
How to tell if you have this one
Check for bottles labeled 'DANONE¿ DAIRY DRINK NUT AND CEREAL 7.7 FL OZ (229mL)' with UPC 36632 01421. The product was sold between October 2016 and January 2017.
- Brand
Dannon- Product
DANONE¿ DAIRY DRINK NUT AND CEREAL 7.7 FL OZ (229mL) bottles, UPC 36632 01421- Category
Food
What to do — step by step
Check Product Label
Look for the UPC code 36632 01421 on the bottle.
Where it went and when
Where it was distributed
Distributed in 18 states.
FDA distribution: “Arizona, California, Colorado, Connecticut, Florida, Georgia, Illinois, Indiana, Kansas, Massachusetts, Michigan, North Carolina, New Jersey, New Mexico, New York, Pennsylvania, Texas, Utah” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arizona, California, Colorado, Connecticut, Florida, Georgia, Illinois, Indiana, Kansas, Massachusetts, Michigan, New Jersey, New Mexico, New York, North Carolina, Pennsylvania, Texas, Utah.
Recall timeline
FDA terminated this recall 17 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
What should I do if I have this product?
The recall does not require immediate action; check the product label and UPC code to confirm if it's affected.
Is there a risk of serious injury?
No, this is an allergen labeling issue, not a physical hazard.
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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-1440-2017 (January 6, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1440-2017 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.