Food Recall Check
Class II · Moderate risk Completed Initiated Aug 3, 2026 (2 months ago)

Protein Cereal Cocoa Crunch recall

Recalled by Nutrient Foods, LLC · Reno, NV, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Soy not declared in the contains statement.

Undeclared allergen: Soy

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

Protein Cereal Cocoa Crunch. Shelf stable, ready to eat cereal product. 25-year shelf life, metalized poly pillow pouch. Net wt.8.9 oz (252g). 1 pillow pouch per kit. Nutrient, 110 Woodland Ave Reno, NV 89523. No UPC Not for individual retail sale

Quantity: 16 kits

Food: Chocolate & candy Pasta, rice & grains Salads, sandwiches & prepared foods

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.

Best if used By on package: 030651, Best if Used by on Kit: 030951

Where it was sold

Florida Indiana Massachusetts Maryland Missouri North Carolina New Jersey Oklahoma Pennsylvania Texas

FDA's distribution note: Product was distributed to the following states: FL, IN, MD, MA, MO, NJ, NC, OK, PA, and TX.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to soy; for anyone else the product is generally not a safety concern. FDA lists this recall as completed: 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
Nutrient Foods, LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Aug 3, 2026
In FDA report of
Aug 26, 2026
FDA recall number
H-1231-2026 · event 99580
Official record
FDA enforcement report search

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