Food Recall Check
Class II · Moderate risk Terminated Initiated Feb 13, 2019 (8 years ago)

Big Daddy s Bold Cheese Pizza recall

Recalled by Schwan's Global Supply Chain, Inc., Specialy Foods Plant · Marshall, MN, United States

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

Why it was recalled

Cheese pizza may contain plastic pieces.

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

Big Daddy s Bold Cheese Pizza, item No. 78985. 3-Pack. Contains 9-44.53 oz. Pizzas. Net Wt. 25.04 Lbs. (11.36 kg) For Institutional Use. Cook Before Serving. Keep Frozen. Manufactured by: SPC Global Supply Chain, Inc. Marshall, MN 56258

Quantity: 8038 cases (3-3 packs per case or 9 pizzas per case)

Food: Cheese

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.

Date Code that begins with 35901823. The date code can be found printed in large dot-matrix print on the side of the master case.

Where it was sold

Arkansas Arizona California Colorado Connecticut Illinois Kentucky Massachusetts Michigan Minnesota Missouri Montana New Jersey New York Ohio Oklahoma Oregon Pennsylvania Texas Utah Virginia Washington Wisconsin

FDA's distribution note: AR, AZ, CA, CO, CT, IL, KY, MA, MI, MN, MO, MT, NJ, NY, OH, OK, OR,PA, TX, UT, VA, WA, WI

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
Schwan's Global Supply Chain, Inc., Specialy Foods Plant
Initiated by
Voluntary: Firm initiated
Recall initiated
Feb 13, 2019
In FDA report of
Mar 13, 2019
Terminated
Jun 20, 2019
FDA recall number
F-1140-2019 · event 82186
Official record
FDA enforcement report search

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