Class IITerminated in FDA datasetRecall initiated Jul 22, 2017

Hy-Vee, Cheese Pizza, 12'' Traditional Crust

Recalling firm: D & D Foods, Inc.

Why it was recalled

Product contains soy lecithin, but soy is not declared on the product's Contains statement and soy lecithin is not declared on the ingredient list

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Sep 7, 2017.

Check your package

Compare the exact product and package details with the label you have.

ProductHy-Vee, Cheese Pizza, 12'' Traditional Crust, UPC 288900 908996, Net Wt. 26 oz (1 lb 10 oz) 1.62 lb (737 g), West Des Moines, IA
Package size26 oz
UPC288900908996

FDA code information

Best if Used by Dates: 04-23-2017 thru 07-26-2017

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Hy-Vee, Cheese Pizza, 12'' Traditional Crust, UPC 288900 908996, Net Wt. 26 oz (1 lb 10 oz) 1.62 lb (737 g), West Des Moines, IA

Extracted codes and context

TypeCode / valueContext
UPC288900908996Hy-Vee, Cheese Pizza, 12'' Traditional Crust, UPC 288900 908996, Net Wt. 26 oz (1 lb 10 oz) 1.62 lb (737 g), West Des Moines, IA

Original FDA recall reason

Product contains soy lecithin, but soy is not declared on the product's Contains statement and soy lecithin is not declared on the ingredient list

Recall details

Recall number
F-3389-2017
Event ID
77814
FDA status
Terminated
Initiated
Jul 22, 2017
Reported
Aug 30, 2017
Classified
Aug 18, 2017
Terminated
Sep 7, 2017
Quantity
471/4 pizzas/cases
Location
Omaha, NE, United States
Initiation type
Voluntary: Firm initiated
Notification
E-Mail

Where it was distributed

The product was distributed to retail grocery stores in the Minneapolis and St. Paul metro area.

FDA source record · F-3389-2017

Data updated September 16, 2026. View official FDA data ↗

Follow official FDA and manufacturer guidance.