Food Recall Check
Class II · Moderate risk Terminated Initiated Dec 11, 2017 (9 years ago)

Rosemary Poppyseed crackers recall

Recalled by Lovejoy Bakers Inc · Portland, OR, United States

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

Why it was recalled

Rosemary Poppyseed crackers, net wt. 6 oz, are recalled due to undeclared wheat. Flour was declared but wheat was not declared in the Ingredients statement.

Undeclared allergen: 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

Rosemary Poppyseed crackers, net wt. 6 oz., packaged in clear poly bag with a twist tie. No UPC code. The label is read in parts: "***Ingredients: Flour, Baking Powder, Salt, Extra Virgin Olive Oil, Fresh Rosemary, Poppyseeds. This bag may contain one or more of the following allergens: Soy, Wheat Flour, Eggs, Milk/Dairy, Peanuts, Tree Nuts***.

Quantity: 6 (6 oz.) bags, 36 oz.

Food: Chips & snacks

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.

Expiration date: 12/18/17

Where it was sold

Oregon

FDA's distribution note: in OR only

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 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
Lovejoy Bakers Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Dec 11, 2017
In FDA report of
Jan 3, 2018
Terminated
Dec 29, 2017
FDA recall number
F-0517-2018 · event 78737
Official record
FDA enforcement report search

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