The Hampton Grocer
Reason Product may be contaminated with Salmonella.
Zeke's Daddy's Granola recall
Recalled by BBF Massachusetts LLC · Greenfield, MA, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Product contains undeclared almond and cashew.
Undeclared allergen: Tree nuts
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
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
Quantity: 177 cases
Food: Pasta, rice & grains
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Product Code: ACZD30 Best By Date: 10/29/2025 Case GTIN Barcode: 00860992000323
Where it was sold
New Jersey
FDA's distribution note: NJ
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to tree nuts; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- BBF Massachusetts LLC
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- May 9, 2025
- In FDA report of
- May 28, 2025
- Terminated
- Sep 30, 2025
- FDA recall number
- F-0810-2025 · event 96864
- Official record
- FDA enforcement report search
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