Zerto Fontal Cheese UPC 20565300000 sliced in store and sold by the pound wrapped in plastic wrap
Summary
The FDA issued a Class I for Zerto Fontal Cheese UPC 20565300000 sliced in store and sold by the pound wrappe by Whole Foods Market Brand 365, Llc. Reason: Undeclared egg sourced from egg lysozyme.
Details
Source
Food Recall
External ID
F-0092-2023
Action Date
2022-11-09
Status
Terminated
Category
food
Product Description
Zerto Fontal Cheese UPC 20565300000 sliced in store and sold by the pound wrapped in plastic wrap
Lot/Code Info: sell by dates 9/28/2022 through 10/20/2022, and were available for purchase in stores from 9/7/2022 through 9/29/2022
Quantity Affected: 213 units
Reason for Recall
Undeclared egg sourced from egg lysozyme
Distribution
Connecticut, New Jersey and New York
Type: Voluntary: Firm initiated
Recall Initiated: 2022-09-30
Company
Austin, TX
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 58 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Whole Foods Market Brand 365, Llc has 7 FDA actions in our database, including 7 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 (Whole Foods Market Brand 365, Llc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Whole Foods Market Brand 365, Llc have FDA actions?
Whole Foods Market Brand 365, Llc has 7 FDA actions in our database, including 7 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0092-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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