CLASS I Food recall · Reported 3 Dec 2025 · FDA Enforcement Report
Face Rock Creamery Vampire Slayer Garlic Cheddar recalled by FRC
FRC is recalling Face Rock Creamery Vampire Slayer Garlic Cheddar, distributed in Oregon. The recall was initiated on 14 Nov 2025 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- H-0212-2026
- FDA event ID
- 97999
- Recalling firm
- FRC, Bandon, OR
- Brand
- Face Rock
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 14 Nov 2025
- FDA classified
- 26 Nov 2025
- Reported
- 3 Dec 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Listeria
- Product category
- Ready Meals
Timeline
| 14 Nov 2025 | Recall initiated by company | |
| 26 Nov 2025 | Classified by FDA | +12 days |
| 3 Dec 2025 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
FDA environmental sample identified the presence of Listeria monocytogenes in the processing area where cheese was packaged.
Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.
Product as listed by the FDA
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.
Where it was distributed
Distributed in Oregon only.
Questions about this recall
Why was it recalled?
FDA environmental sample identified the presence of Listeria monocytogenes in the processing area where cheese was packaged.
Which lots are affected?
Use By 110426.
Where was it sold?
Distributed in Oregon only.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.