Food Recall Check
Class I · High risk Terminated Initiated Aug 11, 2017 (9 years ago)

OPA by Litehouse Ranch recall

Recalled by Litehouse Inc · Sandpoint, ID, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

OPA by Litehouse Ranch was recalled due to undeclared egg.

Undeclared allergen: Egg

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

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***".

Quantity: 742 cases (6 bottles per case)

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

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

Where it was sold

California Colorado Iowa North Dakota Nebraska Oregon Washington

FDA's distribution note: distributed in CA, CO, IA, ND, NE, OR, and WA.

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to egg; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Litehouse Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Aug 11, 2017
In FDA report of
Sep 13, 2017
Terminated
Dec 5, 2017
FDA recall number
F-3514-2017 · event 77945
Official record
FDA enforcement report search

Other recalls by Litehouse Inc