Aldi Choceur Dark Chocolate Bars Recall: Almond Allergen Risk
Aldi recalls Choceur Dark Chocolate Bars (5.29 oz, 20 units/case) due to undeclared almond pieces, a treenut allergen. Consumers should check best-by date (July 24, 2018).
Use caution until it’s fixed
ALDI has voluntarily recalled Choceur Dark Chocolate Bars due to the potential presence of almond pieces, which are an undeclared treenut allergen.
Contact the company
What happened, in plain English
Aldi is recalling Choceur Dark Chocolate Bars because they may contain almond pieces, which are a treenut allergen not declared on the label. This poses a risk for people with almond or tree nut allergies. Read more at govinfonow.com/recall/19982-aldi-choceur-dark-chocolate-bars-recall-almond-allergen-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/19982-aldi-choceur-dark-chocolate-bars-recall-almond-allergen-risk · Updated October 7, 2026 · FDA enforcement record: FDA #F-0555-2018
Cite this page
“Aldi Choceur Dark Chocolate Bars Recall: Almond Allergen Risk.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/19982-aldi-choceur-dark-chocolate-bars-recall-almond-allergen-risk. Based on FDA recall #F-0555-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0555-2018%22&limit=1).
Why it’s dangerous
The chocolate bars may contain almond pieces that are not declared as an allergen. This can cause allergic reactions in people sensitive to almonds or tree nuts, which may include hives, swelling, or anaphylaxis.
Who’s affected
People with almond or tree nut allergies are at risk. The recall affects consumers who purchased these chocolate bars from stores that sold them before the best-by date of July 24, 2018.
How to tell if you have this one
Check for the product name 'Choceur Dark Chocolate Bars', size 5.29 oz, and best-by date of July 24, 2018. The recall covers 20 units per case.
- Brand
Aldi- Category
Food
What to do — step by step
Check Product Details
Look for the product name 'Choceur Dark Chocolate Bars', size 5.29 oz, and best-by date of July 24, 2018.
Where it went and when
Where it was distributed
Distributed in 11 states.
FDA distribution: “Domestic: OH, IN, WI, NY, MI, IL, MD, CT, GA, FL, TX No foreign or VA/DOD” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Connecticut, Florida, Georgia, Illinois, Indiana, Maryland, Michigan, New York, Ohio, Texas, Wisconsin.
Recall timeline
FDA terminated this recall 58 days after the firm started it.
- Firm started the recall
- Published in FDA’s Enforcement Report
- FDA classified it Class I
- 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-0555-2018 (December 5, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0555-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 7, 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.