Food Recall Check
Class II · Moderate risk Terminated Initiated Jul 18, 2023 (3 years ago)

Prima Guida Traditional Homestyle Sheeted Pizza Dough recall

Recalled by Cassanos Inc · Dayton, OH, United States

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

Why it was recalled

Undeclared Allergen - Soy Flour

Undeclared allergen: Soy

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

Prima Guida Traditional Homestyle Sheeted Pizza Dough: packaged as 7in, 8in, 9in, 10in (regular), 10in (thin), 12in (thin), 12in (regular), 14 in (regular), 14in (thin), 16in (thin), 16in (regular), 18in

Quantity: 24575 cases total

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.

Lot: 154, 156, 157, 158, 159, 160, 172, 177, 180, 181, 184, 187, 188, 189, 191, 192 Expiration Date: 12/02/23, 12/04/23, 12/05/23, 12/06/23, 12/07/23, 12/08/23, 12/20/23, 12/25/23, 12/28/23, 12/29/23, 01/01/24, 01/04/24, 01/05/24, 01/06/24, 01/08/24, 01/09/24 Product No. 2657, 4037, 4032, 2804, 1375, 1377, 4038, 1376, 4030, 1378, 4031, 4042

Where it was sold

Colorado Florida Illinois Indiana Kentucky Michigan Ohio Pennsylvania West Virginia

FDA's distribution note: Distributed to: CO, FL, IN, IL, KY, MI, OH, PA, 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. The risk from an undeclared allergen is to people allergic to soy; 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
Cassanos Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Jul 18, 2023
In FDA report of
Aug 9, 2023
Terminated
Sep 27, 2023
FDA recall number
F-1347-2023 · event 92726
Official record
FDA enforcement report search

Also recalled with it (13 more products)

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

Showing 12 of 13.

Other recalls by Cassanos Inc