FDA Recall United States Terminated Historical recordClass I
WFM Purchasing, LP
- Product
- Whatcom Farmhouse- Sliced and packaged in deli plastic wrap…
- Published
- December 3, 2025
- Distribution
- Washington and Oregon
WFM Purchasing, LP Recall: Undeclared Fish and Egg Allergen
United States
OngoingClass I
- Company
- WFM Purchasing, LP
- Product
- Brussel Sprouts & Kale Slaw
- Recall date
- December 31, 2025
- Source
- FDA
Reason for recall
Undeclared Fish and Egg Allergen
- - Recall initiated
- - Reported by source
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Brussel Sprouts & Kale Slaw | Not published in this source record | 88 units | No code |
Distribution
- New York
- New Jersey and Virginia
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- H-0403-2026
- Event ID
- 98249
- Status
- Ongoing
- Classification
- Class I
- Company
- WFM Purchasing, LP
- Product description
- Brussel Sprouts & Kale Slaw
- Quantity
- 88 units
- Reason
- Undeclared Fish and Egg Allergen
- Recall initiation date
- December 31, 2025
- Report date
- January 21, 2026
- Classification date
- Not published in this source record
- Termination date
- Not terminated as of this source record
- Distribution pattern
- New York, New Jersey and Virginia
- UPC, lot, and code information
- No code
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: WFM Purchasing, LP
Other recalls from WFM Purchasing, LP
FDA Recall United States Terminated Historical recordClass I
WFM Purchasing, LP
- Product
- Whatcom Blue Sliced cheese; Sliced and packaged in deli plas…
- Published
- December 3, 2025
- Distribution
- Washington and Oregon
FDA Recall United States Ongoing Historical recordClass I
WFM Purchasing, LP
- Product
- Whole Foods Market Blueberry Almond Granola, PLU 86032, pack…
- Published
- October 8, 2025
- Distribution
- One retail store in Philadelphia, PA.
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 "Ongoing." 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?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
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