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: Twin Sisters Creamery's recall of cheese products due to WSDA testing that identified potential STEC and E. coli O103 contamination. Whole Foods Market received affected products through distributor Peterson Company and sold them by weight with store-generated labels.
United States
TerminatedClass I
- Company
- WFM Purchasing, LP
- Product
- Whatcom Blue Sliced cheese; Sliced and packaged in deli plas…
- Recall date
- October 27, 2025
- Terminated
- February 6, 2026
- Source
- FDA
Reason for recall
Twin Sisters Creamery's recall of cheese products due to WSDA testing that identified potential STEC and E. coli O103 contamination. Whole Foods Market received affected products through distributor Peterson Company and sold them by weight with store-generated labels.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Whatcom Blue Sliced cheese; Sliced and packaged in deli plastic wrap with Whole Foods Scale labels. | Not published in this source record | 411 lbs total | PLU 20667900000 Sell-by Date: 10/27/2025 11/16/2025 |
Distribution
- Washington and Oregon
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- H-0210-2026
- Event ID
- 97931
- Status
- Terminated
- Classification
- Class I
- Company
- WFM Purchasing, LP
- Product description
- Whatcom Blue Sliced cheese; Sliced and packaged in deli plastic wrap with Whole Foods Scale labels.
- Quantity
- 411 lbs total
- Reason
- Twin Sisters Creamery's recall of cheese products due to WSDA testing that identified potential STEC and E. coli O103 contamination. Whole Foods Market received affected products through distributor Peterson Company and sold them by weight with store-generated labels.
- Recall initiation date
- October 27, 2025
- Report date
- December 3, 2025
- Classification date
- Not published in this source record
- Termination date
- February 6, 2026
- Distribution pattern
- Washington and Oregon
- UPC, lot, and code information
- PLU 20667900000 Sell-by Date: 10/27/2025 11/16/2025
- 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
Other products recalled under this same event
This recall shares FDA event ID 97931 with 1 other product entry in Public Health Trace.
Responsible company: WFM Purchasing, LP
Other recalls from WFM Purchasing, LP
FDA Recall United States Ongoing 2026 recordClass I
WFM Purchasing, LP
- Product
- Brussel Sprouts & Kale Slaw
- Published
- January 21, 2026
- Distribution
- New York, New Jersey and Virginia
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
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 "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?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
