Food Recall Check
Class II · Moderate risk Terminated Initiated Jan 13, 2015 (12 years ago)

Mint Bar refrigerated recall

Recalled by My Sweet Ol' Etcetera · Ashland, OR, United States

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

Why it was recalled

Mint Bar is recalled due to undeclared wheat and soy lecithin

Undeclared allergens: Soy 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

Mint Bar, refrigerated, single slice wrapped in cellophane, net wt. 8 oz. The product's label read in parts: "***my sweet ol' etcetera bakery***Mint Bar***Ingredients org flour, org. egg, butter (milk), chocolate, sugar, vanilla, peppermint oil, powdered sugar, butter (milk), cream, melted chocolate***8 oz.***250 oak st. Ashland***541-622-9539***".

Quantity: 36 units

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 1/24/15

Where it was sold

Oregon

FDA's distribution note: Distributed 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 soy, 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
My Sweet Ol' Etcetera
Initiated by
Voluntary: Firm initiated
Recall initiated
Jan 13, 2015
In FDA report of
Feb 25, 2015
Terminated
Feb 27, 2015
FDA recall number
F-1212-2015 · event 70277
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.