Food Recall Check
Class II · Moderate risk Terminated Initiated Jan 26, 2022 (5 years ago)

Kirkland Signature Organic Soy Non-Dairy Beverage Vanilla recall

Recalled by SunOpta Grains and Foods Inc. · Eden Prairie, MN, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Product that did not meet quality standards was released in error. Complaints of spoilage received.

These are failures of the safety steps that keep food safe - cooking, pasteurising, keeping cold, sealing - even when no contaminant has yet been found. All processing & sanitation problems recalls.

What was recalled

Kirkland Signature Organic Soy Non-Dairy Beverage Vanilla; 12- 32 oz. cartons (note- 12 count consumer display case) SunOpta Item number 1243803 Individual Carton UPC: 0 96619 99861 6; 12 x 32 oz. container carton UPC: 096619 49000 4 Ambient, keep refrigerated after opening. Best if used within 7 10 days after opening, not to be used as infant formula. Distributed by: Costco Wholesale Corporation P.O. Box 34535 Seattle, WA 98124

Quantity: 11821341E - 8112 cases; 11821342E - 3963 cases

Food: Juice & beverages

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

07 DEC 2022 11821341E XX:XX; 08 DEC 2022 11821342E XX:XX

Where it was sold

Arizona California Washington

FDA's distribution note: AZ, CA, WA

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
SunOpta Grains and Foods Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Jan 26, 2022
In FDA report of
Feb 9, 2022
Terminated
May 11, 2022
FDA recall number
F-0631-2022 · event 89491
Official record
FDA enforcement report search

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