Item# 28855 Whatcom Blue, Twin Sisters Creamery brand, product is packed in Cryovac and each package weighs 5oz-6oz. The
Summary
The FDA issued a Class I for Item# 28855 Whatcom Blue, Twin Sisters Creamery brand, product is packed in Cryo by Peterson Company Inc. Reason: Item #28855 Whatcom Blue is recalled due to E. coli O103:H2.
Details
Source
Food Recall
External ID
H-0197-2026
Action Date
2025-11-26
Status
Terminated
Category
food
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.
Lot/Code Info: 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
Quantity Affected: 18 cases (16 pieces per case) or 288 pieces
Reason for Recall
Item #28855 Whatcom Blue is recalled due to E. coli O103:H2
Distribution
Press release indicates products were distributed in CO, ID, OR, and WA. Firm confirmed no product was distributed in CO.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-10-25
Company
Auburn, WA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 33 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Peterson Company Inc has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Peterson Company Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Peterson Company Inc have FDA actions?
Peterson Company Inc has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0197-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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