FDA Recall United States Terminated Historical recordClass II
Grand Canyon Foods International LLC.
- Product
- Southwestern Gourmet Prickly Pear Popcorn Grand Canyon Foods…
- Published
- May 30, 2018
- Distribution
- Product distributed to retail stores in…
Grand Canyon Foods International LLC. Recall: An FDA inspection revealed products that contained Yellow 5 and soy lecithin failed to declare the presence of Yellow 5 and soy.
United States
TerminatedClass II
- Company
- Grand Canyon Foods International LLC.
- Product
- Southwestern Gourmet Butter Popcorn Grand Canyon Foods, Phoe…
- Recall date
- April 16, 2018
- Terminated
- August 17, 2018
- Source
- FDA
Reason for recall
An FDA inspection revealed products that contained Yellow 5 and soy lecithin failed to declare the presence of Yellow 5 and soy.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Southwestern Gourmet Butter Popcorn Grand Canyon Foods, Phoenix, AZ | Not published in this source record | 898 bags | All best by dates between 04/09/2018 to 10/09/2018 |
Distribution
- Product distributed to retail stores in AZ
- CA
- CO
- CT
- FL
- GA
- IA
- ID
- IL
- IN
- KS
- KY
- LA
- MI
- MT
- NC
- NH
- NM
- OK
- OR
- SC
- SD
- UT
- VA
- WA
- WI
- and WY
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1493-2018
- Event ID
- 79902
- Status
- Terminated
- Classification
- Class II
- Company
- Grand Canyon Foods International LLC.
- Product description
- Southwestern Gourmet Butter Popcorn Grand Canyon Foods, Phoenix, AZ
- Quantity
- 898 bags
- Reason
- An FDA inspection revealed products that contained Yellow 5 and soy lecithin failed to declare the presence of Yellow 5 and soy.
- Recall initiation date
- April 16, 2018
- Report date
- May 30, 2018
- Classification date
- Not published in this source record
- Termination date
- August 17, 2018
- Distribution pattern
- Product distributed to retail stores in AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MI, MT, NC, NH, NM, OK, OR, SC, SD, UT, VA, WA, WI, and WY
- UPC, lot, and code information
- All best by dates between 04/09/2018 to 10/09/2018
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 79902 with 1 other product entry in Public Health Trace.
Responsible company: Grand Canyon Foods International LLC.
Other recalls from Grand Canyon Foods International LLC.
FDA Recall United States Terminated Historical recordClass II
Grand Canyon Foods International LLC.
- Product
- Southwestern Gourmet Prickly Pear Popcorn Grand Canyon Foods…
- Published
- May 30, 2018
- Distribution
- Product distributed to retail stores in…
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 |
|---|---|
| Arizona | 1 |
| California | 1 |
| Colorado | 1 |
| Connecticut | 1 |
| Florida | 1 |
| Georgia | 1 |
| Iowa | 1 |
| Idaho | 1 |
| Illinois | 1 |
| Indiana | 1 |
| Kansas | 1 |
| Kentucky | 1 |
| Louisiana | 1 |
| Michigan | 1 |
| Montana | 1 |
| North Carolina | 1 |
| New Hampshire | 1 |
| New Mexico | 1 |
| Oklahoma | 1 |
| Oregon | 1 |
| South Carolina | 1 |
| South Dakota | 1 |
| Utah | 1 |
| Virginia | 1 |
| Washington | 1 |
| Wisconsin | 1 |
| Wyoming | 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.
