Class IITerminated in FDA datasetAug 24, 2017

Big Win Butter Popcorn

Recalling firm: Dedinas Franzak Enterprises dba Cheeze Kurls Inc.c.

Why it was recalled

Dedinas Franzak Enterprises dba Cheeze Kurls Inc. initiated a voluntary recall of Big Win Butter Popcorn, 5 oz., Butter Popcorn Artificially Flavored due to undeclared allergen milk.

Check the codes ↓

The exact product

Big Win Butter Popcorn, 5 oz., Butter Popcorn Artificially Flavored; Uncle Ray's 10 oz., Gourmet Select 12 oz., Gold Emblem 5 oz., and Spartan 8 oz.

Check the codes

Compare these FDA-provided codes, lot numbers or dates with the product you have.

Match the product, size and code together. A similar name alone does not identify your batch.

Original FDA code information

Big Win 5oz 16FEB2018 and 01MAR2018 - UPC 011822584920 distributed in Maryland, Pennsylvania, and California. Uncle Rays 10oz 30NOV2017  UPC 614156061992 distributed in Michigan. Gourmet Select 12oz 24NOV2017  UPC 899788002432 distributed in Wisconsin. Gold Emblem 5oz 24NOV2017, 01DEC2017 and 30DEC2017 - UPC 05042844879 distributed in California, Indiana, Virginia, Pennsylvania, Texas, Alabama, New Jersey, South Carolina, and Florida retail stores. Spartan 8oz 01SEP2017  UPC 011213027395 distributed in Michigan.

TypeCode / valueContext
UPC011213027395 Jersey, South Carolina, and Florida retail stores. Spartan 8oz 01SEP2017  UPC 011213027395 distributed in Michigan.
UPC011822584920Big Win 5oz 16FEB2018 and 01MAR2018 - UPC 011822584920 distributed in Maryland, Pennsylvania, and California. Uncle Rays 10oz 30NOV2017  UPC 614156061992 distributed in Mic
UPC614156061992ted in Maryland, Pennsylvania, and California. Uncle Rays 10oz 30NOV2017  UPC 614156061992 distributed in Michigan. Gourmet Select 12oz 24NOV2017  UPC 899788002432 distributed in Wisconsin. Gold Emblem 5oz 24N
UPC899788002432 UPC 614156061992 distributed in Michigan. Gourmet Select 12oz 24NOV2017  UPC 899788002432 distributed in Wisconsin. Gold Emblem 5oz 24NOV2017, 01DEC2017 and 30DEC2017 - UPC 05042844879 distributed in Californi

Recall details

Recall number
F-3583-2017
Event ID
78006
FDA status
Terminated
Initiated
Aug 24, 2017
Reported
Sep 27, 2017
Classified
Sep 21, 2017
Terminated
Jan 16, 2018
Quantity
23,020 units
Location
Grand Rapids, MI, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Domestic only: California, Indiana, Virginia, Pennsylvania, Texas, Alabama, New Jersey, South Carolina, Florida, Maryland, Michigan and Wisconsin No Foreign or VA/DOD customers

FDA source record · F-3583-2017

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

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.