Food Recall Check
Class II · Moderate risk Terminated Initiated Jun 8, 2023 (3 years ago)

Churritos Corn Flour sticks recall

Recalled by Botanas Michoacanas · Portland, OR, United States

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

Why it was recalled

The product labels include a Contains statement that did not disclose sesame for the product that contains sesame. Sesame is included Ingredient statement.

A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.

What was recalled

Churritos Corn Flour sticks, shelf stable, 6 months shelf life, packed in a rectangular shape clear polypropylene bag with net wt.11 oz (311.845g.), UPC# 6-0972233599-7. Product labeled in part, "***BOTANAS MICHOACANS CHURRITOS CORN FLOUR STICKS***Best By:***Ingredients: Corn Flour, wheat flour (niacin, reduced iron, thiamine monoltrate, riboflavin, folic acid) water, salt, sesame seen, corn oil, canola oil. Contains WHEAT. BOTANAS MICHOACANAS PORTLAND, OR 97206***NET WT. 11oz (311.845g)***6-0972233599-7***".

Quantity: 40 -20 piece 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.

Affected product has BEST BY of 6/01/23 to 12/06/23.

Where it was sold

California Oregon

FDA's distribution note: Product was distributed in OR and CA.

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. 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
Botanas Michoacanas
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 8, 2023
In FDA report of
Jul 26, 2023
Terminated
Nov 14, 2024
FDA recall number
F-1250-2023 · event 92517
Official record
FDA enforcement report search

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