peterson company incfoodHigh PriorityExpired

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.

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. was recalled because item #28855 whatcom blue is recalled due to e. coli o103:h2. This recall appears to be closed, but the historical details remain useful for verification.

By RecallRadar Editorial Team

Sourced from FDA. Last verified April 15, 2026.

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Key facts

Date announced
November 26, 2025
Source agency
FDA

This recall involves safety concerns. Take action promptly.

Plain-English Summary

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. was recalled because item #28855 whatcom blue is recalled due to e. coli o103:h2. This recall appears to be closed, but the historical details remain useful for verification.

Is This Recall Still Active?

Status: No - Expired

This recall is no longer active. You can still review details here for historical reference and confirmation.

What's Being Recalled

Quoted source excerpt from the official notice.

Item #28855 Whatcom Blue is recalled due to E. coli O103:H2

Quick Info

Key facts from the official notice, kept in the article flow for easy cross-checking.

Brand
Peterson company inc
Category
food
Source agency
FDA
Announced
November 26, 2025
Country
US
Status
Expired

Who's Affected

Specific models and identifiers listed in the source notice:

Model #1

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

Technical model codes are manufacturer identifiers. Match both the product name and model code from your device settings, label, or packaging.

What You Should Do

Follow the remedy path from the official notice using the exact model and serial details above.

  1. 1Stop using the affected product until you verify whether your item is impacted.
  2. 2Check the official recall notice and match your model, lot, or serial details.
  3. 3Follow the official instructions for repair, replacement, refund, or disposal.

This program has ended. The official source page may no longer be available.

Source & Verification

This page summarizes the official notice and keeps key facts easy to verify.

Official source
FDA
Announced by source
November 26, 2025
Last reviewed by RecallRadar
April 15, 2026

Frequently Asked Questions

Am I affected by this recall?

Check the affected models section on this page. The official notice currently lists 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.

What is the remedy for this recall?

Follow the official instructions for repair, replacement, refund, or disposal on the peterson company inc recall page.

Where can I verify recall details?

Use the official source link in this page to confirm dates, eligibility, and next steps: https://api.fda.gov/food/enforcement.json?search=recall_number:H-0197-2026&limit=1

Keep browsing with these internal hubs: peterson company inc recall hub and Food & Drug recall hub.

Official Resources

Use these primary sources for final eligibility and claim instructions.

View official notice from FDA

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