Ruthies Cashew Raisin Breakfast Cookie
Reason Ruthies Cashew Raisin Breakfast Cookie is recalled because butter and half & half are declared but milk is NOT declared on label.
Ruthies Cranberry Orange Breakfast Cookie recall
Recalled by Wholesale Baking, Inc. · Salem, OR, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Ruthies Cranberry Orange Breakfast Cookie is recalled because butter (cream) is declared but milk is NOT declared on label.
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
Ruthies Cranberry Orange Breakfast Cookie, individually wrapped in plastic, net wt. 4.9 oz. The product is labeled in parts: "***Ruthies Cranberry Orange Breakfast COOKIE***INGREDIENTS***Butter (pasteurized cream, salt)***Contains the following allergens: Wheat, Eggs***NET WT. 4.9 Oz***Manufactured for Ruthie's, LLC***www.ruthiescookies.com******(888) 7-RUTHIE***".
Quantity: 30 cases/24 pieces per case
Food: Berries Bread & bakery
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.
no codes
Where it was sold
Oregon
FDA's distribution note: distributed directly to one sole consignee in Oregon
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
- Wholesale Baking, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Feb 21, 2013
- In FDA report of
- Apr 3, 2013
- Terminated
- Apr 16, 2013
- FDA recall number
- F-1249-2013 · event 64443
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
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