Haagen-Dazs Dark Chocolate Ice Cream Bars Recall: Nuts Found in Packaging
Nestle USA recalls Haagen-Dazs Dark Chocolate Ice Cream Bars due to nuts found in packaging. Consumers should check for nuts in the bars and contact the company for details.
Lower-risk recall
Firm received two complaints of finding a Haagen-Dazs Vanilla Milk Almond Bar found in Chocolate Dark Chocolate bar package. Nuts are visible on the bar.
Contact the company
What happened, in plain English
Nestle USA is recalling Haagen-Dazs Chocolate Dark Chocolate Ice Cream Bars after complaints about finding nuts in the packaging. This poses a risk for people with nut allergies who might consume the bars. Read more at govinfonow.com/recall/22008-haagen-dazs-dark-chocolate-ice-cream-bars-recall-nuts-found.
Source Summary by GovInfoNow · govinfonow.com/recall/22008-haagen-dazs-dark-chocolate-ice-cream-bars-recall-nuts-found · Updated October 8, 2026 · FDA enforcement record: FDA #F-1826-2017
Cite this page
“Haagen-Dazs Dark Chocolate Ice Cream Bars Recall: Nuts Found in Packaging.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/22008-haagen-dazs-dark-chocolate-ice-cream-bars-recall-nuts-found. Based on FDA recall #F-1826-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1826-2017%22&limit=1).
Why it’s dangerous
The bars contain visible nuts in the packaging, which could be ingested by someone with a nut allergy. This is a potential hazard for allergic individuals who might not notice the nuts in the product.
Who’s affected
People with nut allergies who consume the recalled bars may be at risk. The recall affects bars sold in the U.S. between specific dates.
How to tell if you have this one
Check for Haagen-Dazs Chocolate Dark Chocolate Ice Cream Bars with a best by date of December 10, 2017 or earlier. The product code is 6345 580411B.
- Brand
Nestle USA- Category
Food
What to do — step by step
Check for Nuts
Inspect the bars for visible nuts in the packaging, as this is the hazard identified in the recall.
Where it went and when
Where it was distributed
Distributed in 7 states and D.C..
FDA distribution: “CT; DC; DE; MD; NC; NJ; PA; VA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Connecticut, Delaware, District of Columbia, Maryland, New Jersey, North Carolina, Pennsylvania, Virginia.
Recall timeline
FDA terminated this recall 21 days after the firm started it.
- Firm started the recall
- FDA classified it Class II
- FDA terminated the recall
- 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 #F-1826-2017 (March 10, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1826-2017 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.