FDA Recall United States Terminated Historical recordClass I
Whole Foods Market Brand 365, Llc
- Product
- Whole Foods Market Dipping Caramel, PLU 34888 sold by the po…
- Published
- November 16, 2022
- Distribution
- NE, CO, and KS
Whole Foods Market Brand 365, Llc Recall: Undeclared milk and egg
United States
TerminatedClass I
- Company
- Whole Foods Market Brand 365, Llc
- Product
- Whole Foods Market Cookies and Cream Single Layer Cake 8 inc…
- Recall date
- November 9, 2021
- Terminated
- December 8, 2021
- Source
- FDA
Reason for recall
Undeclared milk and egg
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Whole Foods Market Cookies and Cream Single Layer Cake 8 inch NET WT 3lb 0 oz. (1361g) PLU: 39544 packaged in a clear plastic dome | Not published in this source record | 12 units | Packed on 11/08/21, Sell By 11/13/21 |
Distribution
- Colorado
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0246-2022
- Event ID
- 89065
- Status
- Terminated
- Classification
- Class I
- Company
- Whole Foods Market Brand 365, Llc
- Product description
- Whole Foods Market Cookies and Cream Single Layer Cake 8 inch NET WT 3lb 0 oz. (1361g) PLU: 39544 packaged in a clear plastic dome
- Quantity
- 12 units
- Reason
- Undeclared milk and egg
- Recall initiation date
- November 9, 2021
- Report date
- December 15, 2021
- Classification date
- Not published in this source record
- Termination date
- December 8, 2021
- Distribution pattern
- Colorado
- UPC, lot, and code information
- Packed on 11/08/21, Sell By 11/13/21
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Other
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Whole Foods Market Brand 365, Llc
Other recalls from Whole Foods Market Brand 365, Llc
FDA Recall United States Terminated Historical recordClass I
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- Product
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- Published
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- Distribution
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FDA Recall United States Terminated Historical recordClass I
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- Product
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- Published
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- Distribution
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Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
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