Food Recall Check
Class II · Moderate risk Terminated Initiated Feb 12, 2020 (7 years ago)

Coburn Farms Snackers recall

Recalled by Great Lakes Cheese Co Inc · Hiram, OH, United States

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

Why it was recalled

Coburn Farms 4.5oz Snackers is being recalled due to a labeling error leading to undeclared peanut.

Undeclared allergen: Peanut

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

Coburn Farms Snackers, Sharp Yellow Cheddar Cheese, Cherry Juice Infused Dried Cranberries & Roasted Sea Salted Cashews, 3 Pack, Net Wt 4.5 oz (127.5g) 3-1.5 oz (42.5g) packs, Keep Refrigerated. UPC 51933-36243. Distributed By: Save-A-Lot Food Stores, Ltd., Earth City, MO 63045

Quantity: 1572 units

Food: Cheese Nuts & seeds Chips & snacks Berries Juice & beverages

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.

Use By April 24, 2020

Where it was sold

Florida Iowa Illinois Indiana Kansas Kentucky Michigan Missouri Mississippi Ohio Tennessee Virginia Wisconsin West Virginia

FDA's distribution note: Save-A-Lot Retail Stores located in FL, IA, IL, IN, KS, KY, MI, MO, MS,OH, TN, VA, WV, WI

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 peanut; 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
Great Lakes Cheese Co Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Feb 12, 2020
In FDA report of
Mar 4, 2020
Terminated
May 1, 2020
FDA recall number
F-0800-2020 · event 84976
Official record
FDA enforcement report search

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