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Lower risk Food recall · FDA · Published May 23, 2026

Bazzini Dark Chocolate Coconut Almond Bites Recall: Undeclared Peanuts

Bazz: Dark Chocolate Coconut Almond Bites (3.17oz pouches) recalled due to undeclared peanuts. Consumers should check package codes B15354-B15363 for affected items.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #H-1228-2026FoodBazzini ›
Official FDA recall photos · click to enlarge
✎ GovInfoNow plain-language explainer

Bazzini LLC is recalling Dark Chocolate Coconut Almond Bites because they contain undeclared peanuts. This poses a risk for people with peanut allergies who may react to the peanuts. Read more at govinfonow.com/recall/445571-bazzini-dark-chocolate-coconut-almond-bites-recall-undeclared-peanuts.

Source Summary by GovInfoNow · govinfonow.com/recall/445571-bazzini-dark-chocolate-coconut-almond-bites-recall-undeclared-peanuts · Updated August 27, 2026 · Official notice: FDA #H-1228-2026

Cite this page

“Bazzini Dark Chocolate Coconut Almond Bites Recall: Undeclared Peanuts.” GovInfoNow, updated August 27, 2026. https://govinfonow.com/recall/445571-bazzini-dark-chocolate-coconut-almond-bites-recall-undeclared-peanuts. Based on FDA recall #H-1228-2026.

The FDA announced on May 23, 2026, that Bazzini LLC is voluntarily recalling Dark Chocolate Coconut Almond Bites due to undeclared peanuts. The Class I recall affects 1,382,916 pieces distributed to Washington.

How to tell if you have it

  • Brand: Bazzini
  • Product: Dark Chocolate Coconut Almond Bites, 3.17oz, Plastic Pouches
  • Lot codes: B15354, B15356, B15357, B15360, B15361, B15363
  • Distribution: Washington

The hazard

The product contains undeclared peanuts, which poses a risk to individuals with peanut allergies. The FDA classified this as a Class I recall.

Context

GovInfoNow's records show Bazzini LLC has issued four other recalls since October 6, 2018. Recent similar recalls include the Fayus OLA-OLA Pounded Groundnuts Recall on June 19, 2026, and the Karns Mini Dark Chocolate Raspberry Cups Recall on January 30, 2026.

How to tell if you have this one

Check the package for the following codes: B15354, B15356, B15357, B15360, B15361, or B15363. The product is sold in 3.17oz plastic pouches, 10 per case.

  • Brand
    Bazzini
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Package Codes

    Look for the package codes B15354, B15356, B15357, B15360, B15361, or B15363 on the product.

Where it went and when

Where it was distributed

Distributed in Washington.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: yesWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “The product was distributed to WA.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Washington.

Recall timeline

FDA published this recall 3 months after the firm started it.

1. Firm started the recall: May 23, 202612. FDA classified it Class I: Aug 12, 202623. Published in FDA’s Enforcement Report: Aug 19, 202634. Added to GovInfoNow: Aug 27, 202642026
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report
  4. Added to GovInfoNow

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

From the GovInfoNow team · based on the FDA notice · How we make summaries

Do I need to stop using this product?

No action is required beyond checking the package codes. The recall does not require immediate disposal.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #H-1228-2026 (May 23, 2026)
  • Plain-language summary written by qwen3:4b on August 27, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA