Face Rock Creamery Vampire Slayer Garlic Cheddar

FRC INC has recalled Face Rock Creamery Vampire Slayer Garlic Cheddar, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on December 3, 2025 and was initiated on November 14, 2025. It is classified as a Class I recall, which means there is a reasonable chance that using this product could cause serious health problems or death.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers Face Rock Creamery Vampire Slayer Garlic Cheddar, with approximately 16/6oz units or 6lbs. affected. The company behind the recall is FRC INC, based in Bandon, OR. The FDA describes the product as: “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.”

Why was Face Rock Creamery Vampire Slayer Garlic Cheddar recalled?

According to the FDA, the stated reason for the recall is: “FDA environmental sample identified the presence of Listeria monocytogenes in the processing area where cheese was packaged.” In plain terms, this recall relates to Listeria.

Listeria monocytogenes is a bacterium that can grow even at refrigerator temperatures, which makes it a particular concern in ready-to-eat foods. Health authorities warn that it can cause a serious infection called listeriosis, and that pregnant people, newborns, older adults, and those with weakened immune systems are especially vulnerable. This is why products potentially contaminated with Listeria are often recalled quickly.

What should you do?

If you think you may have bought Face Rock Creamery Vampire Slayer Garlic Cheddar, compare it against the product description and identifying codes (Use By 110426.) before using it.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact FRC INC or your local health authority.

About this recall

This recall was distributed in OR. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.