Vans gluten free ORIGINAL WAFFLES recall
Recalled by US Waffle Company, INC. · Liberty, SC, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
The firm was notified, by a consumer, that the product contains undeclared Wheat.
Undeclared allergen: Wheat
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
Vans gluten free ORIGINAL WAFFLES, NET WT. 9 OZ (255G), INGREDIENTS: GLUTEN FREE BLEND (BROWN RICE FLOUR, POTATO STARCH, RICE FLOUR, SOYFLOUR), WATER, EXPELLER PRESSED CANOLA OIL***CONTAINS SOY***DISTRIBUTED BY: VAN'S INTERNATIONAL FOODS OAKBROOK TERRACE, IL 60181 USA***UPC# 0 89947 30206 4
Quantity: N/A
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
BEST BY: JAN 19 2024 UW40193L
Where it was sold
Arizona California Florida Georgia Illinois North Carolina Washington
FDA's distribution note: Product was shipped to the following states: AZ, CA, FL, GA, IL, NC, & WA.
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to wheat; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- US Waffle Company, INC.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jul 3, 2023
- In FDA report of
- Aug 16, 2023
- Terminated
- Dec 8, 2023
- FDA recall number
- F-1382-2023 · event 92638
- Official record
- FDA enforcement report search