Taylor Farms Rotini Pasta Salad Recall: Missing Wheat Allergen Label
Taylor Farms recalls 10oz Rotini Pasta Salad due to missing wheat allergen label. This poses a risk for people with wheat allergies. Consumers should check UPC WO2017019 for affected items.
Lower-risk recall
Retail store employee found that 10 oz. containers of Rotini Salad had the ingredient label for mustard potato salad; thus the allergen of wheat is not declared.
Contact the company
What happened, in plain English
Taylor Farms is recalling 10-ounce Rotini Pasta Salad because it doesn't list wheat as an allergen. This could cause serious allergic reactions in people with wheat allergies. The product was sold in stores with the UPC code WO2017019. Read more at govinfonow.com/recall/22409-taylor-farms-rotini-pasta-salad-recall-missing-wheat-allergen-label.
Source Summary by GovInfoNow · govinfonow.com/recall/22409-taylor-farms-rotini-pasta-salad-recall-missing-wheat-allergen-label · Updated October 8, 2026 · FDA enforcement record: FDA #F-1452-2017
Cite this page
“Taylor Farms Rotini Pasta Salad Recall: Missing Wheat Allergen Label.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/22409-taylor-farms-rotini-pasta-salad-recall-missing-wheat-allergen-label. Based on FDA recall #F-1452-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1452-2017%22&limit=1).
Why it’s dangerous
The salad contains wheat but the label does not declare it as an allergen. This means people with wheat allergies might not know they're consuming it and could have a reaction. The hazard is specific to those with wheat allergies.
Who’s affected
People with wheat allergies who consume this salad may experience allergic reactions. The product was sold in stores with the UPC code WO2017019.
How to tell if you have this one
Check for the UPC code WO2017019 on the clamshell package. The product is a 10-ounce Rotini Pasta Salad sold by Taylor Farms.
- Brand
Taylor Farms- Category
Food
What to do — step by step
Check Product Label
Look for the UPC code WO2017019 on the clamshell package to confirm if it's affected.
Where it went and when
Where it was distributed
Distributed in 5 states.
FDA distribution: “TN, MS, MO, AR, KY” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arkansas, Kentucky, Mississippi, Missouri, Tennessee.
Recall timeline
FDA terminated this recall 2 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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-1452-2017 (January 20, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1452-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 8, 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.