Class IICompletedVoluntary: Firm initiated
Hammond's Candies Since 1920 II, LLC: food recall F-0098-2025
Hammond's Candies Since 1920 II, LLC of Denver, CO recalled Hammond's Dark Chocolate Filled Mini Waffle Cones, packaged in a 4 oz (113g) Stand-Up Resealable Pouch. Item Number:… Reason: Undeclared allergen: milk. The FDA listed it as Class II in its Enforcement Report dated Nov 13, 2024; distribution: nationwide.
Record status as published: Completed. 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
- Hammond's Dark Chocolate Filled Mini Waffle Cones, packaged in a 4 oz (113g) Stand-Up Resealable Pouch. Item Number: FC23212; UPC 6 91355 90513 5. Label declares ***CONTAINS: WHEAT, SOY, TREE NUTS (COCONUT)***PACKAGED IN A FACILITY THAT PROCESSES EGG, MILK, MUSTARD, PEANUTS, SESAME, SOY, SULFITES, TREENUTS, WHEAT.
- Product quantity
- 29,844 units
- Reason for recall
- Undeclared allergen: milk
- Codes, lots and dates on the package
- Lot Number: LN0525453 USE BY: 03/10/2025 USE BY: 03/11/2025 USE BY: 03/20/2025 USE BY: 04/01/2025 USE BY: 05/08/2025 USE BY: 05/20/2025 Lot Number: LN0524629 USE BY: 11/14/2024 USE BY: 12/14/2024 Lot Number: LN0525155 USE BY: 01/01/2025 USE BY: 01/07/2025 USE BY: 03/01/2025
- Distribution pattern
- Nationwide: AL, AR, AZ, CA, CO, DE, FL, GA, IA, IL, IN, KS, KY, MA, MD, MI, MN, MO, MT, NC, NH, NJ, NM, NV, NY, OK, OR, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY, Washington, D.C.
- Recalling firm
- Hammond's Candies Since 1920 II, LLC, Denver, CO
- 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
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Aug 30, 2024 |
| Classified by the FDA | Nov 1, 2024 |
| Published in the Enforcement Report | Nov 13, 2024 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0098-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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