Class IITerminatedVoluntary: Firm initiated
D. Coluccio & Sons Inc.: food recall F-0531-2025
D. Coluccio & Sons Inc. of Brooklyn, NY recalled COLUSSI CANTUCCINI CHOCOLATE DROPS COOKIES. Reason: Contains undeclared visible almonds. The FDA listed it as Class II in its Enforcement Report dated Feb 12, 2025; distribution: Delaware, Florida, Georgia, Massachusetts, Nevada, New York, Pennsylvania.
Record status as published: Terminated (terminated Aug 6, 2025). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- COLUSSI CANTUCCINI CHOCOLATE DROPS COOKIES
- Product quantity
- 1944 units
- Reason for recall
- Contains undeclared visible almonds
- Codes, lots and dates on the package
- UPC 8002590006020 lot # 3540152 BBD 15-01-2025 lot # L354150 BBD 29-05-2025
- Distribution pattern
- NY, PA, MA, FL, GA, DE, NV
- Recalling firm
- D. Coluccio & Sons Inc., Brooklyn, NY
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Jan 21, 2025 |
| Classified by the FDA | Feb 6, 2025 |
| Published in the Enforcement Report | Feb 12, 2025 |
| Terminated | Aug 6, 2025 |
Other recalls by D. Coluccio & Sons Inc.
- H-0366-2026 · Jan 14, 2026 · Class II — Contains elevated levels of hydrocyanic acid
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0531-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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