Kirkland Signature Organic Soy Non-Dairy Beverage Vanilla; 12- 32 oz. cartons (note- 12 count consumer display case)
Summary
The FDA issued a Class II for Kirkland Signature Organic Soy Non-Dairy Beverage Vanilla; 12- 32 oz. cartons ( by SunOpta Grains and Foods Inc.. Reason: Product that did not meet quality standards was released in error. Complaints of spoilage received..
Details
Source
Food Recall
External ID
F-0631-2022
Action Date
2022-02-09
Status
Terminated
Category
food
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
Lot/Code Info: 07 DEC 2022 11821341E XX:XX; 08 DEC 2022 11821342E XX:XX
Quantity Affected: 11821341E - 8112 cases; 11821342E - 3963 cases
Reason for Recall
Product that did not meet quality standards was released in error. Complaints of spoilage received.
Distribution
AZ, CA, WA
Type: Voluntary: Firm initiated
Recall Initiated: 2022-01-26
Company
Eden Prairie, MN
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 112 food recalls issued in the same week, part of 204 food-related FDA actions this month.
SunOpta Grains and Foods Inc. has 18 FDA actions in our database, including 18 recalls.
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 (SunOpta Grains and Foods Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does SunOpta Grains and Foods Inc. have FDA actions?
SunOpta Grains and Foods Inc. has 18 FDA actions in our database, including 18 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0631-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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