Food Recall Check
Class I · High risk Terminated Initiated Oct 5, 2015 (11 years ago)

Snack Out Loud Sea Salt Crunchy Bean Snacks recall

Recalled by Fresca Foods, Incorporated · Louisville, CO, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Fresca Foods conducted a recall on Snack Out Loud Sea Salt flavored Crunchy Bean Snacks due to ranch flavored product being packaged in the sea salt bags, which contain undeclared milk.

Undeclared allergen: Milk

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

Snack Out Loud Sea Salt Crunchy Bean Snacks 1.2 OZ Single Serve Units.

Quantity: 56 cases, 1792 pouches, 1.2 oz each

Food: Chips & snacks

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.

lot #63361, UPC #760055900037

Where it was sold

Nationwide.

California Colorado Virginia

FDA's distribution note: Distributed nationwide to CA and CO. No foreign/VA/govt/military.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to milk; 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
Fresca Foods, Incorporated
Initiated by
Voluntary: Firm initiated
Recall initiated
Oct 5, 2015
In FDA report of
Nov 4, 2015
Terminated
Dec 8, 2015
FDA recall number
F-0125-2016 · event 72348
Official record
FDA enforcement report search

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