Food Recall Check
Class II · Moderate risk Terminated Initiated Jun 5, 2017 (9 years ago)

Carrot Cake Slice recall

Recalled by Albertsons Inc · Boise, ID, United States

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

Why it was recalled

Discovered through the complaint process that the ingredient list for carrot cake slices did not include walnuts in the ingredient or allergen statement. Nuts are visible through packaging.

Undeclared allergen: Tree nuts

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

Carrot Cake Slice: Net Wt. 0 LB 7 OZ (198 g). Cake is assembled, iced, sliced and packaged at store level. Sliced wrapped individually in clear plastic clamshell and sold in bakery department. UPC Code: 0222132-000000 Sold under Albertsons Companies retail banners of Vons, Pavilions, Lucky and Albertsons.

Quantity: 191,885 cake slices

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.

All sell thru codes

Where it was sold

California

FDA's distribution note: Retail stores in 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. The risk from an undeclared allergen is to people allergic to tree nuts; 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
Albertsons Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 5, 2017
In FDA report of
Jul 12, 2017
Terminated
Jul 12, 2017
FDA recall number
F-2412-2017 · event 77452
Official record
FDA enforcement report search

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