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***".
Class I - DangerousWhat Should You Do?
- Check if you have this product: The following codes are observed on the lid: Best by OCT 24 17. 13948
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Litehouse Inc
- Reason for Recall:
- OPA by Litehouse Ranch was recalled due to undeclared egg.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full 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***".
Product Codes/Lot Numbers:
The following codes are observed on the lid: Best by OCT 24 17. 13948
Distribution:
Distributed in: CA, CO, IA, ND, NE, OR, WA
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: F-3514-2017
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