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Food FDA Class I Terminated Pathogen contamination

VAMPIRE SLAYER Garlic Cheddar Cheese Curds, net wt. 6 oz. Product is package in a sealed plastic cup with lid. UPC on 6oz. retail cup: 8 51222 00528 7. FaceRockCreamery.com MASTER CASE's label is read in parts: Item No. 240062 Vampire Slayer Curds 12/6oz., net wt. 4.5 lbs. Face Rock Creamery 680 2n

Face Rock Creamery LLC Published Jul 16, 2025

Risk level

Class I

Dangerous or defective — could cause serious health problems or death.

Severity score 90/100

What should you do?

  • Check whether you have this product, using the lot codes, UPCs, and dates listed below.
  • Do not eat, serve, or sell the affected product.
  • Return it to the place of purchase for a refund, or throw it away in a sealed bag so people and animals can’t get to it.
  • Contact Face Rock Creamery LLC or your place of purchase with questions, and see the source record below for full details.
Reason for recall

Potential to be contaminated with Listeria monocytogenes

Hazards

Listeria monocytogenes · primary

Affected products (1)

VAMPIRE SLAYER Garlic Cheddar Cheese Curds, net wt. 6 oz. Product is package in a sealed plastic cup with lid. UPC on 6oz. retail cup: 8 51222 00528 7. FaceRockCreamery.com MASTER CASE's label is read in parts: Item No. 240062 Vampire Slayer Curds 12/6oz., net wt. 4.5 lbs. Face Rock Creamery 680 2nd St. SE Bandon, OR 97411.

260 cases (12/6oz. cups per case)

Lot codes: numbers, number
Code info: Lot numbers: 20250519VS01 and 20250519VS02. Use By: 08292025 Lot number breaks down as: 2025 = Year 05 = Month 19 = Day of Month VS = Cheese type code 01 or 02 = Production (Vat)

Affected areas

CaliforniaOregon

Timeline

  1. Initiated
    Jun 19, 2025
  2. Published
    Jul 16, 2025
  3. Terminated
    Nov 26, 2025
Recall number
H-0214-2025
Agency
U.S. Food and Drug Administration
Country
US
Source data (openFDA JSON) About FDA enforcement reports

FDA records come from the openFDA food enforcement-report dataset — the agency's full weekly enforcement list. Most entries are not issued as consumer press releases, so they won't appear on fda.gov/recalls or in a web search. The source record link above resolves this exact recall by its number.