RecallHawk
Class I Recall

WFM 365 Organic Creamy Caesar, 12oz, UPC#99482490290, Keep Refrigerated. Bottled in USA. Distributed by: Whole Foods Mar

Vanlaw Food Products, Inc

Summary

The FDA issued a Class I for WFM 365 Organic Creamy Caesar, 12oz, UPC#99482490290, Keep Refrigerated. Bottled by Vanlaw Food Products, Inc. Reason: Undeclared allergens, wheat and soy..

Details

Source

Food Recall

External ID

F-1006-2022

Action Date

2022-04-27

Status

Terminated

Category

food

Product Description

WFM 365 Organic Creamy Caesar, 12oz, UPC#99482490290, Keep Refrigerated. Bottled in USA. Distributed by: Whole Foods Market Austin, TX

Lot/Code Info: Lot Code: BB 11/17/22, which indicates that the product is best by 11/17/2022.

Quantity Affected: 702 Cases

Reason for Recall

Undeclared allergens, wheat and soy.

Distribution

NH, NY, TX

Type: Voluntary: Firm initiated

Recall Initiated: 2022-04-04

Company

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 29 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 I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

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-1006-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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