Lower riskFood recall · FDA · Published January 21, 2025
Coluccio Chocolate Drops Cookies Recall: Undeclared Almonds
D. Coluccio & Sons recalls chocolate drops cookies with undeclared visible almonds. Consumers should check UPC 8002590006020 and lot numbers for affected items.
“Coluccio Chocolate Drops Cookies Recall: Undeclared Almonds.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/8327-coluccio-chocolate-drops-cookies-recall-undeclared-almonds. Based on FDA recall #F-0531-2025 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0531-2025%22&limit=1).
D. Coluccio & Sons Inc. recalled COLUSSI CANTUCCINI CHOCOLATE DROPS COOKIES due to undeclared almonds, the FDA said on Jan. 21, 2025. The voluntary Class II recall affects 1,944 units distributed in NY, PA, MA, FL, GA, DE, and NV.
How to tell if you have it
Brand: Coluccio
Product: COLUSSI CANTUCCINI CHOCOLATE DROPS COOKIES
UPC: 8002590006020
Lot #3540152, BBD 15-01-2025
Lot #L354150, BBD 29-05-2025
The hazard
The product contains undeclared visible almonds, posing an allergy risk to consumers with almond sensitivities. The FDA classified the recall as Class II.
Context
GovInfoNow's records show D. Coluccio & Sons Inc. has one other recall on record since Dec. 14, 2025: a Dec. 14, 2025, Sapori Amaretti Almonds Recall for elevated hydrocyanic acid risk. Other recent recalls of similar products include a May 23, 2026, Bazzini Dark Chocolate Coconut Almond Bites Recall for undeclared peanuts, a May 6, 2026, Albertsons Oatmeal Raisin Cookies Recall for undeclared almonds, and a Dec. 20, 2025, Fran's PureBar Almondmilk Chocolate Recall for undeclared hazelnut hazard.
How to tell if you have this one
Check for the UPC 8002590006020 and lot numbers 3540152 BBD 15-01-2025 or L354150 BBD 29-05-2025 on the packaging.
Brand
Coluccio
Product
COLUSSI CANTUCCINI CHOCOLATE DROPS COOKIES
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Details
Look for the UPC 8002590006020 and lot numbers 3540152 BBD 15-01-2025 or L354150 BBD 29-05-2025 on the packaging.
Where it went and when
Where it was distributed
Distributed in 7 states.
Listed by the agency
Not listed
FDA distribution: “NY, PA, MA, FL, GA, DE, NV” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Delaware, Florida, Georgia, Massachusetts, Nevada, New York, Pennsylvania.
Recall timeline
FDA terminated this recall 6 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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-0531-2025 (January 21, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0531-2025 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 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.