Class IITerminated in FDA datasetRecall initiated Jan 26, 2022

Kirkland Signature Organic Soy Non-Dairy Beverage Vanilla; 12- 32 oz. cartons (note- 12 count…

Recalling firm: SunOpta Grains and Foods Inc.

Why it was recalled

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

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: May 11, 2022.

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ProductKirkland 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
Package size32 oz
UPC096619490004, 096619998616

FDA code information

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

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Full FDA record and distribution details

Original product description

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

Extracted codes and context

TypeCode / valueContext
UPC0966194900043 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 fo
UPC096619998616 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

Original FDA recall reason

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

Recall details

Recall number
F-0631-2022
Event ID
89491
FDA status
Terminated
Initiated
Jan 26, 2022
Reported
Feb 9, 2022
Classified
Feb 3, 2022
Terminated
May 11, 2022
Quantity
11821341E - 8112 cases; 11821342E - 3963 cases
Location
Eden Prairie, MN, United States
Initiation type
Voluntary: Firm initiated
Notification
Telephone

Where it was distributed

AZ, CA, WA

FDA source record · F-0631-2022

Data updated September 16, 2026. View official FDA data ↗

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