Fine Sconehenge Baking Company, ENGLISH SCONE, individually sealed plastic bag
Summary
The FDA issued a Class I for Fine Sconehenge Baking Company, ENGLISH SCONE, individually sealed plastic bag by The Kitchen Garden Co, LLC. Reason: Undeclared allergen; egg.
Details
Source
Food Recall
External ID
F-0310-2024
Action Date
2023-11-08
Status
Terminated
Category
food
Product Description
Fine Sconehenge Baking Company, ENGLISH SCONE, individually sealed plastic bag
Lot/Code Info: Firm does not generate manufacturing codes
Quantity Affected: N/A
Reason for Recall
Undeclared allergen; egg
Distribution
U.S. customers can order scones directly from firm's website. The firm distributes to customers in CA and NV.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-09-12
Company
Camarillo, 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 17 food recalls issued in the same week, part of 204 food-related FDA actions this month.
The Kitchen Garden Co, LLC has 5 FDA actions in our database, including 5 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 (The Kitchen Garden Co, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does The Kitchen Garden Co, LLC have FDA actions?
The Kitchen Garden Co, LLC has 5 FDA actions in our database, including 5 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0310-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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