Food Recall Check
Class II · Moderate risk Terminated Initiated Aug 28, 2012 (14 years ago)

Walnuts 160z Brand Name recall

Recalled by Meijer Distribution, Inc · Grand Rapids, MI, United States

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

Why it was recalled

The firm was notified by a produce manager at one of the store locations that some of the bags from this lot of product contain pecans in addition to walnuts. Pecans are not listed in the ingredient statement and are not called out as an allergen.

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

Product Name: Walnuts 160z. Brand Name: Markets of Meijer Meijer Distribution, Inc. Grand Rapids, MI49544 UPC 8-8692619782-2

Quantity: 1,440 units (60 cases, 24 units/case).

Food: Nuts & seeds

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.

Lot Number: 08 2150

Where it was sold

Illinois Indiana Kentucky Michigan Ohio

FDA's distribution note: Up to 199 Meijer stores located in Illinois, Indiana, Kentucky, Michigan, and Ohio may have received product from Meijer distribution centers.

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
Meijer Distribution, Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Aug 28, 2012
In FDA report of
Oct 3, 2012
Terminated
Aug 27, 2013
FDA recall number
F-2372-2012 · event 63046
Official record
FDA enforcement report search

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