Food Recall Check
Class II · Moderate risk Terminated Initiated May 5, 2015 (11 years ago)

evolution FRESH brand Fresh Berries & Honey recall

Recalled by Flying Food Group - LAW · Harbor City, CA, United States

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

Why it was recalled

Product recalled due to undeclared almonds.

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

evolution FRESH brand Fresh Berries & Honey, Nonfat Greek Yogurt with Strawberries, Blueberries, Pure Honey, & Granola; NET WT 6.5 OZ/184 g; Perishable Keep Refrigerated; SKU 11048364; Made Exclusively For: Evolution Fresh, Inc. 2401 Utah Avenue South Seattle, WA 98134 USA. The product is packaged in clear plastic containers that are segregated into three sections with fruit, granola, and yogurt and honey.

Quantity: 2,568

Food: Milk & dairy Berries

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.

Enjoy By 05 08

Where it was sold

California

FDA's distribution note: 651 stores of 1 consignee located in CA (San Diego and Los Angeles area only). No distribution to other states or foreign countries.

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
Flying Food Group - LAW
Initiated by
Voluntary: Firm initiated
Recall initiated
May 5, 2015
In FDA report of
Jun 17, 2015
Terminated
Oct 30, 2015
FDA recall number
F-2407-2015 · event 71210
Official record
FDA enforcement report search

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