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Item #28855 Whatcom Blue is recalled due to E. coli O103:H2
- Recall initiated
- Reported by source
- Recall terminated
Recalled products
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.
FDA Recall🇺🇸 United StatesTerminatedTerminated: April 1, 2026Historical recordClass I
A map highlighting the states named in the source's distribution description.
Distributed
No data published
Shading reflects state-level totals only, as published by the source. It does not imply
county-level or point-level precision.
Distribution map
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.
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.
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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.
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or product is unsafe beyond what the official source has published.
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