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Disclaimer: Recall Radar is an informational summary of public FDA enforcement reports. It is not medical advice. Always confirm details with the FDA, the company, a pharmacist, or a doctor before making health decisions.

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Class IFood

Dark Chocolate Coconut Almond Bites recall

Summary

Bazzini LLC is recalling Dark Chocolate Coconut Almond Bites (food). According to the FDA report, the reason is: Undeclared peanuts. The FDA rated this a Class I: most serious: there is a reasonable chance the product could cause serious health problems or death. Recall status: Ongoing.

Understanding this recall

What happened

Bazzini is recalling Dark Chocolate Coconut Almond Bites because they contain peanuts that aren't declared on the label.

Why it matters

Peanut is one of the major food allergens. For people with a peanut allergy, even a small amount can cause a reaction ranging from hives and swelling to anaphylaxis, which is life-threatening. If peanut isn't on the label, an allergic person has no warning.

Who should pay attention

People with peanut allergies in Washington state.
Distribution in the FDA report: The product was distributed to WA.

How to check your product

Check the code on the pouch against the codes below.
Codes listed by the FDA: B15354, B15356, B15357, B15360, B15361, B15363

Based only on the FDA enforcement record plus general public-health background on this type of hazard. Not medical advice; if you have symptoms or concerns, contact a doctor or pharmacist.

Details from the FDA report

Product
Dark Chocolate Coconut Almond Bites, 3.17oz, Plastic Pouches, 10 Packages per case.
Reason
Undeclared peanuts
Lot / code info
B15354, B15356, B15357, B15360, B15361, B15363
Quantity
1,382,916 Pieces
Distribution
The product was distributed to WA.
Recalling company
Bazzini LLC, Allentown, PA United States
Recall started
May 23, 2026
FDA report date
August 19, 2026
Classification
Class I: Most serious: there is a reasonable chance the product could cause serious health problems or death.
Voluntary / mandated
Voluntary: Firm initiated
Status
Ongoing
Recall number
H-1228-2026

What to do

View the FDA source record (openFDA) · FDA recalls page

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