Food Recall Check
Class I · High risk Terminated Initiated Mar 25, 2016 (11 years ago)

Fresh Food Market Cranberry Chicken Salad recall

Recalled by The Kroger Co · Cincinnati, OH, United States

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

Why it was recalled

Fresh Food Market Cranberry Chicken Salad is recalled because product may be mislabeled and may contain undeclared pecans, wheat, and soy.

Undeclared allergens: Tree nuts Soy Wheat

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

Fresh Food Market Cranberry Chicken Salad, UPC 207063-4XXXX, various package sizes. Product sold both from bulk service case and self-service case random weight in deli cups. Product is privately labeled and the address is shown as QFC, 10116 NE 8th, Bellevue, WA 98004.

Quantity: 810 lbs.

Food: Berries 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.

Sell by March 28, 2016 and Before

Where it was sold

Oregon Washington

FDA's distribution note: distributed in Oregon and Washington

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 tree nuts, soy, wheat; 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
The Kroger Co
Initiated by
Voluntary: Firm initiated
Recall initiated
Mar 25, 2016
In FDA report of
Sep 28, 2016
Terminated
Mar 29, 2017
FDA recall number
F-2386-2016 · event 73656
Official record
FDA enforcement report search

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