Food Recall Check
Class I · High risk Terminated Initiated Dec 19, 2019 (7 years ago)

Everyday Value Dark Chocolate Caramel Sea Salt Sandwich Cremes recall

Recalled by Whole Foods Market · Austin, TX, United States

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

Why it was recalled

Potential to contain undeclared milk and coconut.

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

365 Everyday Value Dark Chocolate Caramel Sea Salt Sandwich Cremes Net Wt 7.75 oz (220g) UPC 9948247606 Paper carton boxes sold individually

Quantity: 3895 cases

Food: Chocolate & candy Salads, sandwiches & prepared foods

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 05/02/20 through 05/09/20; Lot Codes A201-2 12139, A201-2 22139, A201-2 12149, A201-2 12159, A201-2 12160, A201-2 12179, A201-2 22179, A201-2 12189, A201-2 22189, A201-2 12199, A201-2 22199, A201-2 12209, A201-2 22209, A201-2 12219

Where it was sold

Nationwide.

FDA's distribution note: Nationwide and Canada

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
Whole Foods Market
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 19, 2019
In FDA report of
Feb 5, 2020
Terminated
Jan 28, 2020
FDA recall number
F-0564-2020 · event 84549
Official record
FDA enforcement report search

Also recalled with it (1 more product)

FDA files each product of one recall action separately; these share the same FDA event.

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