CLASS I Food recall · Reported 13 Sep 2017 · FDA Enforcement Report

OPA by Litehouse Ranch recalled

Litehouse is recalling OPA by Litehouse Ranch, distributed in 7 states. The recall was initiated on 11 Aug 2017 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesThe following codes are observed on the lid: Best by OCT 24 17. 13948

Quantity recalled742 cases (6 bottles per case)

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number: F-3514-2017
FDA event ID: 77945
Recalling firm: Litehouse, Sandpoint, ID
Classification: Class I
Status: Terminated
Recall initiated: 11 Aug 2017
FDA classified: 6 Sep 2017
Reported: 13 Sep 2017
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Undeclared Egg
Product category: Sauces & Condiments

Timeline

11 Aug 2017	Recall initiated by company
6 Sep 2017	Classified by FDA	+26 days
13 Sep 2017	Published in enforcement report	+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

OPA by Litehouse Ranch was recalled due to undeclared egg.

Product as listed by the FDA

OPA by Litehouse Ranch, 6/11.25 oz. glass round bottles per case. The retail label listed item #48246 and has the UPC 0 77661 15022 1. The UPC on master case outer label is 01 1 0077661 13948 3. The recalled product's retail label is read in parts: "***OPA BY LITEHOUSE*** ranch *** GREEK YOGURT DRESSING***11.25 FL OZ***48246***CONTAINS: MILK***". The recalled product's master case outer label is read in parts: "***OPA RANCH***KEEP REFRIGERATED***Pack 6/11FL ***Item #:13846***".

Where it was distributed

distributed in CA, CO, IA, ND, NE, OR, and WA.

California Colorado Iowa North Dakota Nebraska Oregon Washington

Questions about this recall

Why was it recalled?

OPA by Litehouse Ranch was recalled due to undeclared egg.

Which lots are affected?

The following codes are observed on the lid: Best by OCT 24 17. 13948

Where was it sold?

distributed in CA, CO, IA, ND, NE, OR, and WA.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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