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Use caution Food recall · FDA · Published June 14, 2016

Mill House Salad Dressing Recall: Undeclared Sulfites

Van Vogt Creations recalls Mill House Salad Dressing & Gourmet Sauce due to undeclared sulfites. Check your bottle if you bought it in WA.

🇺🇸 FDA recall #F-2201-2016FoodMill House ›
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Recalling firmVan Vogt Creations50 Hutchens Hill Rd · Pomeroy, WA 99347-9655
✎ GovInfoNow plain-language explainer

What happened, in plain English

Van Vogt Creations is recalling a small batch of Mill House Salad Dressing & Gourmet Sauce because the label does not list sulfites as an ingredient. This matters because people with sulfite allergies could have a reaction without knowing it. The recall affects only 26 bottles sold at the company's retail store in Washington. Read more at govinfonow.com/recall/23976-mill-house-salad-dressing-recall-undeclared-sulfites.

Source Summary by GovInfoNow · govinfonow.com/recall/23976-mill-house-salad-dressing-recall-undeclared-sulfites · Updated October 9, 2026 · FDA enforcement record: FDA #F-2201-2016

Cite this page

“Mill House Salad Dressing Recall: Undeclared Sulfites.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23976-mill-house-salad-dressing-recall-undeclared-sulfites. Based on FDA recall #F-2201-2016 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2201-2016%22&limit=1).

Why it’s dangerous

The product contains sulfites, but they are not declared on the ingredient label. This omission poses a health risk to individuals who must avoid sulfites due to allergies or sensitivities.

Who’s affected

Consumers who purchased Mill House Salad Dressing & Gourmet Sauce from Van Vogt Creations' retail store in Washington. Individuals with sulfite allergies are at risk of an allergic reaction.

How to tell if you have this one

Look for 12 FL OZ plastic bottles of Mill House Salad Dressing & Gourmet Sauce. Check the label for ingredients including canola oil, garlic, lemon juice, water, salt, and pepper. Verify the Best By date is 4/16/17.

  • Brand
    Mill House
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check your product

    Verify if you have a 12 FL OZ plastic bottle of Mill House Salad Dressing & Gourmet Sauce with a Best By date of 4/16/17.

  2. Avoid consumption

    Do not consume the product if you have a sulfite allergy, as the ingredient is undeclared.

Where it went and when

Where it was distributed

Distributed in Washington.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: yesWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: 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: “Firm's retail store located in WA” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Washington.

Recall timeline

FDA terminated this recall 3 months after the firm started it.

1. Firm started the recall: Jun 14, 201612. FDA classified it Class II: Sep 14, 201623. FDA terminated the recall: Sep 14, 201634. Published in FDA’s Enforcement Report: Sep 21, 201642016
  1. Firm started the recall
  2. FDA classified it Class II
  3. FDA terminated the recall
  4. Published in FDA’s Enforcement Report

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-2201-2016 (June 14, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2201-2016 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b 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