The Vanilla Bean Greek Yogurt 4oz cup is part of the 12-Pack case, Ellenos Greek Yogurt, Grade A Milk, Costco Item Code:
Summary
The FDA issued a Class II for The Vanilla Bean Greek Yogurt 4oz cup is part of the 12-Pack case, Ellenos Greek by REAL GREEK LLC. Reason: Undeclared egg. Lemon Curd yogurt was mis-labeled as Vanilla Bean yogurt and egg is not declared on Vanilla Bean yogurt label..
Details
Source
Food Recall
External ID
F-0889-2023
Action Date
2023-05-24
Status
Terminated
Category
food
Product Description
The Vanilla Bean Greek Yogurt 4oz cup is part of the 12-Pack case, Ellenos Greek Yogurt, Grade A Milk, Costco Item Code: # 1340833. The 12-Pack case has the UPC 8 57290 00617 1. The Vanilla Bean Greek Yogurt 4oz cup has the UPC 8 57290 00620 1. Label declares Ingredients: Yogurt (Grade A Pasteurized Milk, Grade A milk Protein Concentrate***Cane Sugar, Honey, Pure Vanilla Extract, Natural Flavor, Ground Vanilla Beans. Allergen: Contains Milk. Made in a facility that processes Egg, Wheat, and Tree Nuts. Manufactured By: Real Greek LLC, Plant Code 53-74, Federal Way, WA.
Lot/Code Info: Vanilla Bean Yogurt 4oz cup has the Best Before date of 4/23/2023. The 12-pack case has the Best Before date 4/23/2023 and Lot Number 073.
Quantity Affected: 4,016 cases (16,064 cups) were distributed and about 340 cases (1,348 individual cups) were impacted
Reason for Recall
Undeclared egg. Lemon Curd yogurt was mis-labeled as Vanilla Bean yogurt and egg is not declared on Vanilla Bean yogurt label.
Distribution
Distributed in Alaska, Oregon, and Washington.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-04-24
Company
Federal Way, WA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 74 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (REAL GREEK LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does REAL GREEK LLC have FDA actions?
This is the only FDA action we have on record for REAL GREEK LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0889-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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