Food Recall Check
Class II · Moderate risk Terminated Initiated Apr 27, 2016 (10 years ago)

Corn Seasoning Salt Blue Cheese and Herb recall

Recalled by Jacobsen Salt Co. · Portland, OR, United States

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

Why it was recalled

Corn Seasoning Salt Blue Cheese and Herb is recalled because the label declared blue cheese but milk is not declared.

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

Corn Seasoning Salt Blue Cheese and Herb. Plastic bottles, 6 bottles per case. various sizes: Wt. 5.7 oz. The UPC is 8 14417 02089 2. Product is labeled in parts: "***CORN SEASONING SALT BLUE CHEESE & HERB***INGREDIENTS: BLUE CHEESE, JACOBSEN SEA SALT, OREGANO, THYME***Manufactured by Jacobsen Salt Co. Portland, OR 97214***".

Quantity: 2400 units total

Food: Cheese Spices & seasonings

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 code: 89226039, 89226062, 89226081, 89226085; Best Before (Month/Year): 12/2019 or 1/2020

Where it was sold

Mississippi

FDA's distribution note: Mississippi

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 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
Jacobsen Salt Co.
Initiated by
Voluntary: Firm initiated
Recall initiated
Apr 27, 2016
In FDA report of
Jun 1, 2016
Terminated
Feb 1, 2017
FDA recall number
F-1397-2016 · event 74003
Official record
FDA enforcement report search

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