CLASS I Food recall · Reported 28 May 2025 · FDA Enforcement Report

Zeke's Daddy's Granola recalled by BBF Massachusetts

BBF Massachusetts is recalling Zeke's Daddy's Granola, distributed in New Jersey. The recall was initiated on 9 May 2025 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesProduct Code: ACZD30 Best By Date: 10/29/2025 Case GTIN Barcode: 00860992000323
Quantity recalled177 cases

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0810-2025
FDA event ID
96864
Recalling firm
BBF Massachusetts, Greenfield, MA
Classification
Class I
Status
Terminated
Recall initiated
9 May 2025
FDA classified
22 May 2025
Reported
28 May 2025
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Tree Nuts
Product category
Granola Bars

Timeline

9 May 2025Recall initiated by company
22 May 2025Classified by FDA+13 days
28 May 2025Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Product contains undeclared almond and cashew.

Product as listed by the FDA

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

Where it was distributed

NJ

New Jersey

Questions about this recall

Why was it recalled?

Product contains undeclared almond and cashew.

Which lots are affected?

Product Code: ACZD30 Best By Date: 10/29/2025 Case GTIN Barcode: 00860992000323

Where was it sold?

NJ

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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