FDA recall record

REAL GREEK The Vanilla Bean Greek Yogurt 4oz cup is part of the 12-Pack recall — FDA F-0889-2023

Undeclared egg. Lemon Curd yogurt was mis-labeled as Vanilla Bean yogurt and egg is not declared on Vanilla Bean yogurt label.

Class IIclassification
F-0889-2023official record ID
May 24, 2023report date

Recall record at a glance

Official recordF-0889-2023
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmREAL GREEK LLC
Report dateMay 24, 2023
Recall initiation dateApr 24, 2023
Quantity4,016 cases (16,064 cups) were distributed and about 340 cases (1,348 individual cups) were impacted
LocationFederal Way, WA, United States

Official 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.

Why the product was recalled

Undeclared egg. Lemon Curd yogurt was mis-labeled as Vanilla Bean yogurt and egg is not declared on Vanilla Bean yogurt label.

Distribution information

Distributed in Alaska, Oregon, and Washington.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA 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

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