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Lower risk Food recall · FDA · Published January 24, 2017

Market Basket moreBAR Dark Chocolate Peanut Bar Recall: Undeclared Walnuts

DeMoulas Supermarket recalls Market Basket moreBAR Dark Chocolate Peanut bars due to undeclared walnuts. Consumers should check lot numbers for affected items.

🇺🇸 FDA recall #F-2382-2017FoodDeMoulas ›
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Recalling firmDeMoulas Supermarket, Inc.875 East St · Tewksbury, MA 01876-1469
✎ GovInfoNow plain-language explainer

What happened, in plain English

DeMoul: Market Basket moreBAR Dark Chocolate Peanut bars (4.3 oz) are recalled because they contain undeclared walnuts. This poses a risk for people with nut allergies who may react to the walnuts. Read more at govinfonow.com/recall/22399-market-basket-morebar-dark-chocolate-peanut-bar-recall-undeclared-walnuts.

Source Summary by GovInfoNow · govinfonow.com/recall/22399-market-basket-morebar-dark-chocolate-peanut-bar-recall-undeclared-walnuts · Updated October 8, 2026 · FDA enforcement record: FDA #F-2382-2017

Cite this page

“Market Basket moreBAR Dark Chocolate Peanut Bar Recall: Undeclared Walnuts.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/22399-market-basket-morebar-dark-chocolate-peanut-bar-recall-undeclared-walnuts. Based on FDA recall #F-2382-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2382-2017%22&limit=1).

Why it’s dangerous

The bars contain walnuts that are not listed on the label. This can cause allergic reactions in people who are sensitive to nuts, especially if they have a severe allergy.

Who’s affected

People with nut allergies are most at risk from this recall. The product is sold through Market Basket stores.

How to tell if you have this one

Check for the lot number 2176P on the packaging. The product is a 4.3 oz dark chocolate peanut bar sold by Market Basket.

  • Brand
    DeMoulas
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the lot number 2176P on the packaging to confirm if the item is affected.

How this recall unfolded

Recall timeline

FDA terminated this recall 5 months after the firm started it.

1. Firm started the recall: Jan 24, 201712. FDA classified it Class II: Jun 19, 201723. Published in FDA’s Enforcement Report: Jun 28, 201734. FDA terminated the recall: Jun 30, 201742017
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. 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-2382-2017 (January 24, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2382-2017 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA