ASIN B0CY2RDW5T, Amazon Fresh brand, Bake at Home Jumbo Sugar Cookie 30oz, product is frozen dough, and packaged in flex
Summary
The FDA issued a Class I for ASIN B0CY2RDW5T, Amazon Fresh brand, Bake at Home Jumbo Sugar Cookie 30oz, produ by Amazon Retail LLC. Reason: Undeclared egg..
Details
Source
Food Recall
External ID
F-0607-2025
Action Date
2025-03-12
Status
Terminated
Category
food
Product Description
ASIN B0CY2RDW5T, Amazon Fresh brand, Bake at Home Jumbo Sugar Cookie 30oz, product is frozen dough, and packaged in flexible plastic bag. UPC 446472006995.
Lot/Code Info: sold by dates between 2/12/2024 and 1/25/2025.
Quantity Affected: 192 packages (30oz)
Reason for Recall
Undeclared egg.
Distribution
distributed nationwide.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-01-25
Company
Seattle, WA
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 37 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Amazon Retail LLC 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 (Amazon Retail LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Amazon Retail LLC have FDA actions?
Amazon Retail LLC 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-0607-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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