Food Recall Check
Class II · Moderate risk Terminated Initiated Oct 11, 2018 (8 years ago)

Foodstirs Modern Baking recall

Recalled by Foodstirs · Los Angeles, CA, United States

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

Why it was recalled

Individual pouches of Organic Minute Mug Cake Mix Celebration Confetti 4-pack do not declare milk as an allergen. The correct allergen statement is on the outer carton.

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

Foodstirs Modern Baking; Organic Minute Mug Cake Mix Celebration Confetti - 4 - 2.54 oz. (72g) Pouches per carton -Carton Net Wt. 10.16 oz. (288g) Carton UPC; 816524 02789 Master case UPC: 816524 020796

Quantity: 7996 cases (6 cartons per case)

Food: Bread & bakery

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 by dates: 7/30/19, 9/27/19, 11/18/19 and 11/20/2019.

Where it was sold

Arizona California Colorado Georgia Illinois Indiana Kentucky Ohio Oregon Pennsylvania Texas

FDA's distribution note: Distributors in CA, TX, OR, AZ, OH, IL, CO, KY, IN, PA, GA

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
Foodstirs
Initiated by
Voluntary: Firm initiated
Recall initiated
Oct 11, 2018
In FDA report of
Nov 7, 2018
Terminated
Nov 7, 2018
FDA recall number
F-0075-2019 · event 81268
Official record
FDA enforcement report search

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