Pasta Salad 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

Pasta Salad Mix, "10 oz cello bag, Contents: All natural enriched semolina flour, spray dried tomato, spinach and beet powders, water, parsley, celery seed, garlic, paprika, and spices***PURELY AMERICAN 5991 Industrial Park Road, Athens, OH 45701 (800) 359-7873 www.purelyamerican.com" Sold under the brand names: PICNIC AT CAPE MAY UPC 7 92290 00143 9 and PICNIC AT FAIRMOUNT PARK UPC 7 92290 00138 5.

Quantity: 91/10 oz cello bags

Food: Leafy greens & salads Pasta, rice & grains 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 # CA104, ITEM #146, ITEM #143, ITEM #145 and ITEM #138

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-1507-2013 · 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