FDA Recall United States Terminated Historical recordClass II
Tyson Foods Discovery Center
- Product
- Pierre Philly Style Cheesesteak Sandwich, item 1125, 12 unit…
- Published
- November 14, 2018
- Distribution
- United States
Tyson Foods Discovery Center Recall: The firm was notified that they failed to include the allergens milk & wheat in their ingredient statement.
United States
CompletedClass I
- Company
- Tyson Foods Discovery Center
- Product
- Vans gluten free Original 6 WAFFLES NET WT 9 OZ (255g) INGRE…
- Recall date
- April 27, 2018
- Source
- FDA
Reason for recall
The firm was notified that they failed to include the allergens milk & wheat in their ingredient statement.
- - Recall initiated
- - Reported by source
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Vans gluten free Original 6 WAFFLES NET WT 9 OZ (255g) INGREDIENTS:***VAN'S GLUTEN FREE MIX (BROWN RICE FLOUR, POTATO STARCH, RICE FLOUR, SOY FLOUR),***RICE FLOUR,***SUNFLOWER AND/OR SOY LECITHIN***CONTAINS: SOY DISTRIBUTED BY: VAN'S INTERNATIONAL FOODS SAN DIEGO, CA 92154 UPC 0 89947 30206 4 | Not published in this source record | 1,584cs/12/9 oz boxes | Lot Code #A640234710 WL2, BEST BY AUG 22, 2018 |
Distribution
- Product was shipped to the following states: AR
- CA
- CO
- GA
- IL
- MI
- NJ
- NY
- PA
- TX & WI.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1475-2018
- Event ID
- 79999
- Status
- Completed
- Classification
- Class I
- Company
- Tyson Foods Discovery Center
- Product description
- Vans gluten free Original 6 WAFFLES NET WT 9 OZ (255g) INGREDIENTS:***VAN'S GLUTEN FREE MIX (BROWN RICE FLOUR, POTATO STARCH, RICE FLOUR, SOY FLOUR),***RICE FLOUR,***SUNFLOWER AND/OR SOY LECITHIN***CONTAINS: SOY DISTRIBUTED BY: VAN'S INTERNATIONAL FOODS SAN DIEGO, CA 92154 UPC 0 89947 30206 4
- Quantity
- 1,584cs/12/9 oz boxes
- Reason
- The firm was notified that they failed to include the allergens milk & wheat in their ingredient statement.
- Recall initiation date
- April 27, 2018
- Report date
- May 23, 2018
- Classification date
- Not published in this source record
- Termination date
- Not terminated as of this source record
- Distribution pattern
- Product was shipped to the following states: AR, CA, CO, GA, IL, MI, NJ, NY, PA, TX & WI.
- UPC, lot, and code information
- Lot Code #A640234710 WL2, BEST BY AUG 22, 2018
- 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: Tyson Foods Discovery Center
Other recalls from Tyson Foods Discovery Center
FDA Recall United States Terminated Historical recordClass II
Tyson Foods Discovery Center
- Product
- Steak-EZE Philly Cheesesteak Sandwich, item 06433, Net Wt 5.…
- Published
- November 14, 2018
- Distribution
- United States
FDA Recall United States Terminated Historical recordClass II
Tyson Foods Discovery Center
- Product
- TGIF All American Slider, item 5461, 4 cartons of 4 sandwich…
- Published
- November 14, 2018
- Distribution
- United States
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 |
|---|---|
| Arkansas | 1 |
| California | 1 |
| Colorado | 1 |
| Georgia | 1 |
| Illinois | 1 |
| Michigan | 1 |
| New Jersey | 1 |
| New York | 1 |
| Pennsylvania | 1 |
| Texas | 1 |
| Wisconsin | 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 I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
Is this recall still active?
According to FDA, this recall's status is "Completed." 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.
