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Lower risk Food recall · FDA · Published September 14, 2016

Field Day Organic Ranch Dressing Recall: Undeclared Milk and Egg Allergens

Field Day Organic Ranch Dressing in 8 fl oz glass bottles with UPC #042563600242 may contain undeclared milk and egg allergens. Consumers should check the back label for the lot code W210I (best by Jan 28, 2018) to identify affected products.

🇺🇸 FDA recall #F-0677-2017FoodField Day ›
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Recalling firmDrews LLC926 Vermont Rt 103 S · Chester, VT 05143
✎ GovInfoNow plain-language explainer

What happened, in plain English

Field Day Organic Ranch Dressing in 8 fl oz glass bottles with UPC #042563600242 has been recalled because some bottles do not list milk and egg as allergens on the back label. This poses a risk for people with milk or egg allergies who might consume the product without knowing. Read more at govinfonow.com/recall/23210-field-day-organic-ranch-dressing-recall-undeclared-milk-and-egg.

Source Summary by GovInfoNow · govinfonow.com/recall/23210-field-day-organic-ranch-dressing-recall-undeclared-milk-and-egg · Updated October 9, 2026 · FDA enforcement record: FDA #F-0677-2017

Cite this page

“Field Day Organic Ranch Dressing Recall: Undeclared Milk and Egg Allergens.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23210-field-day-organic-ranch-dressing-recall-undeclared-milk-and-egg. Based on FDA recall #F-0677-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0677-2017%22&limit=1).

Why it’s dangerous

The dressing is packaged in glass bottles that sometimes have a back label missing milk and egg allergen declarations. This means people with milk or egg allergies could unknowingly consume the product and experience an allergic reaction.

Who’s affected

People with milk or egg allergies who consume the recalled dressing may be at risk of an allergic reaction. The recall affects consumers who bought the product between the best by date of January 28, 2018, and the current date.

How to tell if you have this one

Check the back label of the bottle for the lot code W210I. The product has a best by date of January 28, 2018, and the UPC number 042563600242.

  • Brand
    Field Day
  • Product
    Field Day Organic Ranch Dressing packaged in an 8 fl. oz. glass bottle, UPC #042563600242. The lot code is located on
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Back Label

    Look for the lot code W210I on the back of the bottle above the label.

Where it went and when

Where it was distributed

Distributed in Illinois.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “IL” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Illinois.

Recall timeline

FDA terminated this recall 11 months after the firm started it.

1. Firm started the recall: Sep 14, 201612. FDA classified it Class I: Dec 8, 201623. Published in FDA’s Enforcement Report: Dec 14, 201634. FDA terminated the recall: Aug 15, 2017420162017
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report
  4. 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-0677-2017 (September 14, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0677-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 9, 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA