FDA Recall United States Terminated Historical recordClass I
Peterson Company Inc
- Product
- Item# 29608 Farmhouse White, Twin Sisters Creamery brand, pr…
- Published
- November 26, 2025
- Distribution
- Press release indicates products were di…
Peterson Company Inc Recall: Item #28855 Whatcom Blue is recalled due to E. coli O103:H2
United States
TerminatedClass I
- Company
- Peterson Company Inc
- Product
- Item# 28855 Whatcom Blue, Twin Sisters Creamery brand, produ…
- Recall date
- October 25, 2025
- Terminated
- April 1, 2026
- Source
- FDA
Reason for recall
Item #28855 Whatcom Blue is recalled due to E. coli O103:H2
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Item# 28855 Whatcom Blue, Twin Sisters Creamery brand, product is packed in Cryovac and each package weighs 5oz-6oz. There are 16 pieces per case. This cheese is made from raw milk. Ingredients: cultured raw cow's milk, salt, enzymes, penicillium roqueforti. Made by Twin Sisters Creamery in Ferndale, WA. Distributed by Peterson Company of Auburn, WA. | Not published in this source record | 18 cases (16 pieces per case) or 288 pieces | MFG Code 761511 MFG Code 775511 MFG Code 781511 MFG Code 793511 761511 = cut on 9/18/2025 775511 = cut on 10/2/2025 781511 = cut on 10/8/2025 793511 = cut on 10/20/2025 |
Distribution
- Press release indicates products were distributed in CO
- ID
- OR
- and WA. Firm confirmed no product was distributed in CO.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- H-0197-2026
- Event ID
- 97881
- Status
- Terminated
- Classification
- Class I
- Company
- Peterson Company Inc
- Product description
- Item# 28855 Whatcom Blue, Twin Sisters Creamery brand, product is packed in Cryovac and each package weighs 5oz-6oz. There are 16 pieces per case. This cheese is made from raw milk. Ingredients: cultured raw cow's milk, salt, enzymes, penicillium roqueforti. Made by Twin Sisters Creamery in Ferndale, WA. Distributed by Peterson Company of Auburn, WA.
- Quantity
- 18 cases (16 pieces per case) or 288 pieces
- Reason
- Item #28855 Whatcom Blue is recalled due to E. coli O103:H2
- Recall initiation date
- October 25, 2025
- Report date
- November 26, 2025
- Classification date
- Not published in this source record
- Termination date
- April 1, 2026
- Distribution pattern
- Press release indicates products were distributed in CO, ID, OR, and WA. Firm confirmed no product was distributed in CO.
- UPC, lot, and code information
- MFG Code 761511 MFG Code 775511 MFG Code 781511 MFG Code 793511 761511 = cut on 9/18/2025 775511 = cut on 10/2/2025 781511 = cut on 10/8/2025 793511 = cut on 10/20/2025
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- 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 97881 with 1 other product entry in Public Health Trace.
Responsible company: Peterson Company Inc
Other recalls from Peterson Company Inc
FDA Recall United States Terminated Historical recordClass I
Peterson Company Inc
- Product
- Item# 29608 Farmhouse White, Twin Sisters Creamery brand, pr…
- Published
- November 26, 2025
- Distribution
- Press release indicates products were di…
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Colorado | 1 |
| Idaho | 1 |
| Oregon | 1 |
| Washington | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
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.
