Dedinas Franzak Enterprises dba Cheeze Kurls Inc.c. Recall: 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.
United States
TerminatedClass II
- Company
- Dedinas Franzak Enterprises dba Cheeze Kurls Inc.c.
- Product
- Big Win Butter Popcorn, 5 oz., Butter Popcorn Artificially F…
- Recall date
- August 24, 2017
- Terminated
- January 16, 2018
- Source
- FDA
Reason for recall
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.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| 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. | Not published in this source record | 23,020 units | 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. |
Distribution
- Domestic only: California
- Indiana
- Virginia
- Pennsylvania
- Texas
- Alabama
- New Jersey
- South Carolina
- Florida
- Maryland
- Michigan and Wisconsin No Foreign or VA/DOD customers
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-3583-2017
- Event ID
- 78006
- Status
- Terminated
- Classification
- Class II
- Company
- Dedinas Franzak Enterprises dba Cheeze Kurls Inc.c.
- Product description
- 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.
- Quantity
- 23,020 units
- Reason
- 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.
- Recall initiation date
- August 24, 2017
- Report date
- September 27, 2017
- Classification date
- Not published in this source record
- Termination date
- January 16, 2018
- Distribution pattern
- Domestic only: California, Indiana, Virginia, Pennsylvania, Texas, Alabama, New Jersey, South Carolina, Florida, Maryland, Michigan and Wisconsin No Foreign or VA/DOD customers
- UPC, lot, and 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.
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Dedinas Franzak Enterprises dba Cheeze Kurls Inc.c.
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Virginia | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
