Class ITerminatedVoluntary: Firm initiated
BBF Massachusetts LLC: food recall F-0810-2025
BBF Massachusetts LLC of Greenfield, MA recalled Zeke's Daddy's Granola; INGREDIENTS: Whole grain rolled oats, maple syrup, expeller pressed canola oil, coconut, brown… Reason: Product contains undeclared almond and cashew. The FDA listed it as Class I in its Enforcement Report dated May 28, 2025; distribution: New Jersey.
Record status as published: Terminated (terminated Sep 30, 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
- Zeke's Daddy's Granola; INGREDIENTS: Whole grain rolled oats, maple syrup, expeller pressed canola oil, coconut, brown sugar, molasses, cinnamon, salt, natural flavor; Contains coconut; Manufactured in a facility that uses peanuts, tree nuts, soy, wheat, sesame, and milk; 30 LBS; ACAI GUYS
- Product quantity
- 177 cases
- Reason for recall
- Product contains undeclared almond and cashew.
- Codes, lots and dates on the package
- Product Code: ACZD30 Best By Date: 10/29/2025 Case GTIN Barcode: 00860992000323
- Distribution pattern
- NJ
- Recalling firm
- BBF Massachusetts LLC, Greenfield, MA
- Classification
- Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | May 9, 2025 |
| Classified by the FDA | May 22, 2025 |
| Published in the Enforcement Report | May 28, 2025 |
| Terminated | Sep 30, 2025 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0810-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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