Food Recall Check
Class II · Moderate risk Terminated Initiated Feb 13, 2013 (14 years ago)

All Natural Ancient Grain Bread recall

Recalled by Rich Products Corp · Buffalo, NY, United States

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

Why it was recalled

Product was manufactured with bulk flour supplied by Dakota Specialty Milling which is being recalled due to reports of metal fragments..

Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.

What was recalled

ALL NATURAL ANCIENT GRAIN BREAD, NET WT. 13.8 OZ. (393 g), PRODUCT OF CANADA, UPC 0 49800 08712 5 (appears on bag), Product Code 08712 --- RICH PRODUCTS CORP., BUFFALO, NY 14213 --- The product is a frozen bread dough packaged in a plastic bag with 24 plastic bags per case. The frozen dough is sold to in-store bakeries and food service customers.

Quantity: Approximately 6,000 cases

Food: 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.

Product produced from July 27, 2012 through February 1, 2013 (Julian Dates 77002209 - 77003302)

Where it was sold

California Illinois Indiana Kansas Michigan Minnesota Missouri North Dakota Nebraska New York Oklahoma Pennsylvania South Dakota Tennessee Texas Virginia Washington Wisconsin

FDA's distribution note: NY, PA, VA, TN, IN, MI, WI, MN, SD, ND, IL, MO, NE, KS, OK, TX, CA, WA

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
Rich Products Corp
Initiated by
Voluntary: Firm initiated
Recall initiated
Feb 13, 2013
In FDA report of
Mar 13, 2013
Terminated
May 15, 2018
FDA recall number
F-1052-2013 · event 64396
Official record
FDA enforcement report search

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