Food Recall Check
Class II · Moderate risk Terminated Initiated May 26, 2023 (3 years ago)

Rudolphs OnYums Onion Flavored Snack Rings recall

Recalled by Rudolph Foods Company · Dallas, TX, United States

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

Why it was recalled

Undeclared wheat and artificial colors (Yellow 6, Yellow Lake 6, Blue 2 Lake, Blue 1 Lake, Red 40 Lake)

Undeclared allergen: Wheat

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

Rudolphs OnYums Onion Flavored Snack Rings 3 oz. UPC 0-24622-57106-9 packaged in metallized film bags, 15 bags per case

Quantity: 39 cases

Food: Chips & snacks Onions

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.

AUG 3 2023 140943D97 Time stamp 02:00 to 04:30

Where it was sold

Arkansas Colorado Iowa Illinois Indiana Kansas Kentucky Minnesota Missouri Montana North Dakota Nebraska Oklahoma South Dakota Tennessee Wisconsin Wyoming

FDA's distribution note: Arkansas, Colorado, Illinois, Indiana, Iowa, Kansas, Kentucky, Minnesota, Missouri, Montana, Nebraska, North Dakota, Oklahoma, South Dakota, Tennessee, Wisconsin, and Wyoming

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 wheat; for anyone else the product is generally not a safety concern. 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
Rudolph Foods Company
Initiated by
Voluntary: Firm initiated
Recall initiated
May 26, 2023
In FDA report of
Jul 5, 2023
Terminated
Apr 9, 2024
FDA recall number
F-1012-2023 · event 92426
Official record
FDA enforcement report search

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