Recall record at a glance
| Official record | F-3514-2017 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Litehouse Inc. |
| Report date | Sep 13, 2017 |
| Recall initiation date | Aug 11, 2017 |
| Quantity | 742 cases (6 bottles per case) |
| Location | Sandpoint, ID, United States |
Official product description
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***".
Why the product was recalled
OPA by Litehouse Ranch was recalled due to undeclared egg.
Distribution information
distributed in CA, CO, IA, ND, NE, OR, and WA.
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Letter.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.