Whole Foods Market Vanilla Short Bread Cookies packaged in clear plastic container with a white scale label applied PLU
Summary
The FDA issued a Class I for Whole Foods Market Vanilla Short Bread Cookies packaged in clear plastic contain by Whole Foods Market Brand 365, Llc. Reason: Undeclared egg.
Details
Source
Food Recall
External ID
F-0806-2022
Action Date
2022-03-09
Status
Terminated
Category
food
Product Description
Whole Foods Market Vanilla Short Bread Cookies packaged in clear plastic container with a white scale label applied PLU 66705
Lot/Code Info: Pack Date: 1/20/22, Sell By Date 2/19/22
Quantity Affected: 23 units
Reason for Recall
Undeclared egg
Distribution
Washington D.C.
Type: Voluntary: Firm initiated
Recall Initiated: 2022-02-03
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 70 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-0806-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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