Lower riskFood recall · FDA · Published September 22, 2022
Treehouse Foods Italian Dressing Recall: Undeclared Soy and Wheat
Treehouse Foods recalls 12-count mixed case of Restaurant Style Italian Dressing due to undeclared soy and wheat. Consumers should check product labels for lot number 42A08092.
“Treehouse Foods Italian Dressing Recall: Undeclared Soy and Wheat.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/12286-treehouse-foods-italian-dressing-recall-undeclared-soy-and-wheat. Based on FDA recall #F-0051-2023 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0051-2023%22&limit=1).
The FDA announced on 2022-09-22 that Treehouse Foods is recalling Tuscan Garden Restaurant Style Italian Dressing due to undeclared soy and wheat. The agency said the product was distributed to one consignee in several states.
How to tell if you have it
Tuscan Garden Restaurant Style Italian Dressing, Net 16 FL OZ (1 PT) 473 mL, Plastic Bottle 12 count mixed case
Lot 42A08092
Best By 08/10/2023
UPC 4099100074871
The hazard
The dressing contains undeclared soy and wheat, which can cause allergic reactions in sensitive individuals. The FDA said the recall is classified as Class II.
Context
GovInfoNow's records show Treehouse Foods has 10 other recalls on record since 2016-05-03. Recent brand recalls include a 2025-04-30 chocolate pudding recall for swollen containers, a 2024-10-17 Good & Gather recall for Listeria risk, and a 2023-10-18 Gluten Free Waffles recall for peanut contamination. Other recent recalls of similar products include Coco's Italian Market Fettuccini Alfredo Recall (2026-02-03), Dreamland Zaatar Chickpea Salad Recall (2026-02-25), and Stuffed Foods Cacio e Pepe Arancini Recall (2025-11-12).
How to tell if you have this one
Check for the product name 'Tuscan Garden Restaurant Style Italian Dressing' on a plastic bottle. Look for the lot number 42A08092 and best-by date of August 10, 2023.
Brand
Treehouse Foods
Product
Tuscan Garden Restaurant Style Italian Dressing , Net 16 FL OZ (1 PT) 473 mL, Plastic Bottle 12 count mixed case
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for the lot number 42A08092 and best-by date of August 10, 2023 on the bottle.
Where it went and when
Where it was distributed
Distributed in 19 states.
Listed by the agency
Not listed
FDA distribution: “The product was distributed to one consignee in several states. Al, IL, PA, MD, GA, NC, NY, MN, TX, WI, VA, OH, IN, MI, CT, FL, KS, TN, CA and MO” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Connecticut, Florida, Georgia, Illinois, Indiana, Kansas, Maryland, Michigan, Minnesota, Missouri, New York, North Carolina, Ohio, Pennsylvania, Tennessee, Texas, Virginia, Wisconsin.
Recall timeline
FDA terminated this recall 5 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #F-0051-2023 (September 22, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0051-2023 to see it in context.
Plain-language summary written by qwen3:4b on October 4, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.