Food Recall Check
Class II · Moderate risk Terminated Initiated Apr 13, 2023 (3 years ago)

Creekside Mallow Chocolate Chip Mint Marshmallows recall

Recalled by Creekside Mallow LLC · Caldwell, ID, United States

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

Why it was recalled

Butterfat is declared in the Ingredients Statement, but MILK is not declared in the Contains statement.

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

Creekside Mallow Chocolate Chip Mint Marshmallows, packed in a Stand Up Flexible Pouch (Bag), Net wt. 3.9oz. UPC 7 09951 63271 0. Manufactured by Creekside Mallow LLC Caldwell, ID. www.creeksidemallow.com. The label declares: INGREDIENTS: CORN SYRUP ***SUGAR, WATER, CHOCOLATE CHIPS (SUGAR, CHOCOLATE LIQUOR, COCOA BUTTER, BUTTERFAT, SOY LECITHIN, NATURAL FLAVOR)***CONTAINS: SOY.

Quantity: 2800 packages

Food: Chocolate & candy

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.

All codes and dates (DDMMYY). New product NOT subject to recall will have the statement "Contains: MILK, SOY".

Where it was sold

Washington

FDA's distribution note: Distributed in Washington.

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 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
Creekside Mallow LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Apr 13, 2023
In FDA report of
May 3, 2023
Terminated
Sep 5, 2023
FDA recall number
F-0751-2023 · event 92135
Official record
FDA enforcement report search

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