Lyle Style Mild Bloody Mary Mix recall
Recalled by Lyle Style · White Salmon, WA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Undeclared Soy. Finished product ingredients statement declares Worcestershire sauce but does not declare sub-ingredients Soy Flavoring and Soy Lecithin.
Undeclared allergen: Soy
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
Lyle Style Mild Bloody Mary Mix, 32oz. glass bottle. UPC code 7 84762 03730 3. The label declares "***Ingredients***Tomato Juice ***lemon***Worcestershire sauce (vinegar, molasses, water, corn sweeteners, caramel coloring, anchovies, natural flavorings)***Made in the Columbia River Gorge - Lyle, Washington***"
Quantity: Total 50 cases for both products
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.
Production dates: 7-28-2025 to 7-28-2026. No lot codes. Product is stickered with Best By Date a year from production date.
Where it was sold
Oregon Washington
FDA's distribution note: Distributed in Oregon and Washington
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to soy; 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
- Lyle Style
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jul 28, 2026
- In FDA report of
- Aug 19, 2026
- Terminated
- Sep 1, 2026
- FDA recall number
- Not assigned yet — FDA has not classified this recall. FDA event ID 99517
- Official record
- FDA enforcement report search