Recall Register

Food recall: OPA by Litehouse Ranch, 6/11.25 oz. glass round bottles per case. The retail label listed item #48246 and has the UPC…

Class I FDA enforcement event 77945. Recall start date: . Status in the FDA record: Terminated. Termination date: .

Reason for recall, in the words of FDA

OPA by Litehouse Ranch was recalled due to undeclared egg.

Class I, in the words of FDA

a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death

Litehouse Inc started this food recall on 11 Aug 2017. The firm address in the FDA record is in Sandpoint, ID. FDA put the recall in Class I. FDA event 77945 has 1 product record. The first FDA enforcement report date is 13 Sep 2017. The record gives the status Terminated, with the termination date 5 Dec 2017.

It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.

FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .

Distribution

In the words of FDA.

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

Recalling firm

Litehouse Inc, Sandpoint, ID.

Recalling firm: The firm that the FDA record names for a recall.

FDA records how the recall started: Voluntary: Firm initiated.

Products

1 product record in the event.

FDA event 77945: product records
Recall numberProductQuantityClassStatusReport date
F-3514-2017OPA 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…742 cases (6 bottles per case)Class ITerminated13 Sep 2017

openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports. Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.

Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.

Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.

Class I: The highest of the three FDA recall classes.

The event in context

Food events that started in 2017
599
Share of these events in Class I
41%
Product records in this event
1Median of the firm: 1
Events of the firm on the register
4

Other events of the firm

Official channels

Cite this page

Recall Register. FDA enforcement event 77945. https://recallregister.com/fda/i/77945/. Source: openFDA enforcement reports. Data through .

Sources

Source
openFDA food enforcement reports
Licence
CC0 1.0
Export date
28 Sep 2026
Newest FDA report date on the register
23 Sep 2026

FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.

Questions

Where was the product distributed?
The FDA record gives this distribution: distributed in CA, CO, IA, ND, NE, OR, and WA.
What quantity of product is in FDA event 77945?
The FDA record gives this quantity: 742 cases (6 bottles per case)
How did the recall start?
The FDA record says: Voluntary: Firm initiated
How many food recalls of 2017 have the same class?
41% of the 599 food events that started in 2017 are in Class I.