Indian River Orange Drop Cookies Mix recall

Recalled by Purely American, Inc. · Athens, OH, United States

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

Why it was recalled

The firm was notified by the Ohio Department of Agriculture that several of their labels are missing the the allergin declaration contains wheat.

A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.

What was recalled

INDIAN RIVER ORANGE DROP COOKIES MIX 17 oz coffee bag Contents: Unbleached white flour; granulated sugar, confectioner's sugar, orange peel, baking powder, and salt***PURELY AMERICAN 5991 Industrial Park Road, Athens, OH 45701 (800) 359-7873 www.purelyamerican.com UPC 7 92290 00135 4

Quantity: 25/17 oz coffee bags

Food: Pasta, rice & grains Bread & bakery 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.

ITEM #135

Where it was sold

Connecticut Delaware Florida Georgia Illinois Indiana Kentucky Maryland Maine Michigan Missouri North Carolina Nebraska New Jersey New York Ohio Pennsylvania South Dakota Virginia West Virginia

FDA's distribution note: Product was shipped to the following states: CT, DE, FL, GA, IL, IN, KY, MD, ME, MI, MO, NC, NE, NJ, NY, OH, PA, SD, VA & WV.

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. 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: Purely American, Inc.
Initiated by: Voluntary: Firm initiated
Recall initiated: Mar 12, 2013
In FDA report of: Jun 19, 2013
Terminated: Jul 31, 2014
FDA recall number: F-1514-2013 · event 64834
Official record: FDA enforcement report search

Also recalled with it (10 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Class II · Moderate risk Terminated Labeling Mar 12, 2013