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Food recall · FDA · Published August 11, 2017

Litehouse Inc recalls OPA by Litehouse Ranch, 6/11.25 oz. glass round bottles per case. The retail label listed item #48246 and has the UPC 0

Litehouse recalls OPA Greek Yogurt Dressing (item #48246) due to undeclared egg. Consumers should check labels for the UPC 077661150221 and avoid products with egg.

🇺🇸 FDA recall #F-3514-2017FoodLitehouse ›
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Contact the company & request your remedy

Recalling firmLitehouse Inc100 Litehouse Dr, N/A · Sandpoint, ID 83864-0528
No email on file for this recall — reach the company by phone or its official page instead.No email on file — write to the address above instead.
✎ GovInfoNow plain-language explainer

What happened, in plain English

Litehouse is recalling OPA Greek Yogurt Dressing bottles that contain undeclared egg. This poses a risk for people with egg allergies who may experience allergic reactions. The product was sold in glass bottles labeled with item #48246 and UPC 077661150221. Read more at govinfonow.com/recall/20517-litehouse-opa-greek-yogurt-dressing-recall-undeclared-egg-hazard.

Source Summary by GovInfoNow · govinfonow.com/recall/20517-litehouse-opa-greek-yogurt-dressing-recall-undeclared-egg-hazard · Updated October 7, 2026 · FDA enforcement record: FDA #F-3514-2017

Cite this page

“Litehouse OPA Greek Yogurt Dressing Recall: Undeclared Egg Hazard.” GovInfoNow, updated October 7, 2026. https://govinfonow.com/recall/20517-litehouse-opa-greek-yogurt-dressing-recall-undeclared-egg-hazard. Based on FDA recall #F-3514-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-3514-2017%22&limit=1).

Why it’s dangerous

The product contains undeclared egg, which can trigger allergic reactions in individuals sensitive to egg. This is a food safety issue that affects consumers with egg allergies who may not have been aware the product contained egg.

Who’s affected

People with egg allergies are at risk of allergic reactions from this product. The recall affects consumers who purchased the OPA Greek Yogurt Dressing bottles labeled with item #48246 and UPC 077661150221.

How to tell if you have this one

Check for the retail label with item #48246 and UPC 077661150221. The product is a 11.25 fl oz glass round bottle sold in cases of six.

  • Brand
    Litehouse
  • Product
    Litehouse Inc recalls OPA by Litehouse Ranch, 6/11.25 oz. glass round bottles per case. The retail label listed item #48246 and has the UPC 0
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Label

    Look for the retail label with item #48246 and UPC 077661150221 on the bottle.

✎ GovInfoNow

Questions people ask

Why is this product being recalled?

The product contains undeclared egg, which can trigger allergic reactions in people with egg allergies.

What should I do if I have this product?

Check the label for item #48246 and UPC 077661150221. If you have the product, avoid it due to the risk of allergic reactions.

Is there a remedy for this product?

The recall does not provide a remedy; consumers should avoid the product if they have the label details.

Take action

Contact Litehouse

We’ve drafted a message you can send Litehouse to request your refund or repair — edit it as you like.

Subject: Recall F-3514-2017 — Litehouse Litehouse Inc recalls OPA by Litehouse Ranch, 6/11.25 oz. glass round bottles per case. T

Hello,

I own a Litehouse Inc recalls OPA by Litehouse Ranch, 6/11.25 oz. glass round bottles per case. The retail label listed item #48246 and has the UPC 0 that is covered by recall F-3514-2017 from Litehouse.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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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-3514-2017 (August 11, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-3514-2017 to see it in context.
  • Plain-language summary written by qwen3:4b on October 7, 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