WFM 365 Organic Creamy Caesar, 12oz, UPC#: 99482490029, Keep Refrigerated. Bottled in USA. Distributed by: Whole Foods M
Summary
The FDA issued a Class II for WFM 365 Organic Creamy Caesar, 12oz, UPC#: 99482490029, Keep Refrigerated. Bottl by Vanlaw Food Products, Inc. Reason: Product does not declare the allergens of wheat and soy on label..
Details
Source
Food Recall
External ID
F-0002-2023
Action Date
2022-10-12
Status
Terminated
Category
food
Product Description
WFM 365 Organic Creamy Caesar, 12oz, UPC#: 99482490029, Keep Refrigerated. Bottled in USA. Distributed by: Whole Foods Market: Austin, TX Expanded recall to include the best if used by date of SEP 21 22 through JUN 06 23 and UPC Code 99482-49027
Lot/Code Info: Lot Code: Top Line Code: 04 06 23, which indicates that the product is best if used by date of SEP 21 22 through JUN 06 23 and UPC Code 99482-49027. Bottom Line Code: A535-1, which is the identification code of the product
Quantity Affected: 31,858 units
Reason for Recall
Product does not declare the allergens of wheat and soy on label.
Distribution
Product was distributed to 4 distribution centers located in FL, WI, CO, and NY. Product was further distributed to Alabama, Connecticut, Georgia, Illinois, Indiana, Iowa, Kansas, Kentucky, Michigan, Minnesota, Mississippi, Missouri, Nebraska, New Jersey, New Mexico, North Carolina, Ohio, South Carolina, Tennessee, Texas, Utah, and Wyoming.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-08-25
Company
Fullerton, CA
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 57 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Vanlaw Food Products, Inc has 2 FDA actions in our database, including 2 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 (Vanlaw Food Products, Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Vanlaw Food Products, Inc have FDA actions?
Vanlaw Food Products, Inc has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0002-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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