St. Benoit French Vanilla Yogurt; from pasture raised Jersey cows. Packaged in glass jar, net wt. 4.75 oz., UPC 6 49241
Summary
The FDA issued a Class I for St. Benoit French Vanilla Yogurt; from pasture raised Jersey cows. Packaged in by Laura Chenel's Chevre, Inc.. Reason: Undeclared Egg..
Details
Source
Food Recall
External ID
F-0912-2022
Action Date
2022-04-06
Status
Terminated
Category
food
Product Description
St. Benoit French Vanilla Yogurt; from pasture raised Jersey cows. Packaged in glass jar, net wt. 4.75 oz., UPC 6 49241 92910 9, St. Benoit Creamery. Sonoma, CA 95476 Certified Organic by CCOF
Lot/Code Info: lot code # 2054, best by date 8/22/2022
Quantity Affected: 752 units
Reason for Recall
Undeclared Egg.
Distribution
Distributed in Alaska, Idaho, Oregon, and Washington
Type: Voluntary: Firm initiated
Recall Initiated: 2022-03-15
Company
Sonoma, CA
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 23 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (Laura Chenel's Chevre, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Laura Chenel's Chevre, Inc. have FDA actions?
This is the only FDA action we have on record for Laura Chenel's Chevre, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0912-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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