Class ITerminatedVoluntary: Firm initiated
FRC INC: food recall H-0212-2026
FRC INC of Bandon, OR recalled Face Rock Creamery Vampire Slayer Garlic Cheddar, net wt. 6oz. Ready to Eat, Refrigerated/ Perishable. Product is… Reason: FDA environmental sample identified the presence of Listeria monocytogenes in the processing area where cheese was packaged. The FDA listed it as Class I in its Enforcement Report dated Dec 3, 2025; distribution: Oregon.
Record status as published: Terminated (terminated Jan 9, 2026). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- Face Rock Creamery Vampire Slayer Garlic Cheddar, net wt. 6oz. Ready to Eat, Refrigerated/ Perishable. Product is packaged in sealed in bag and shrink dipped. UPC 8 51222 00547 8. Face Rock Creamery, 680 2nd St. SE Bandon, OR 97411.
- Product quantity
- 16/6oz units or 6lbs.
- Reason for recall
- FDA environmental sample identified the presence of Listeria monocytogenes in the processing area where cheese was packaged.
- Codes, lots and dates on the package
- Use By 110426.
- Distribution pattern
- Distributed in Oregon only.
- Recalling firm
- FRC INC, Bandon, OR
- Classification
- Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Nov 14, 2025 |
| Classified by the FDA | Nov 26, 2025 |
| Published in the Enforcement Report | Dec 3, 2025 |
| Terminated | Jan 9, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0212-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.