A soft chevre-style cheese. Label reads in part, "*** TUMALO FARMS Artisan Cheeses of Central Oregon Chevita This fresh and mild, soft, white cheese has a great tangy finish www.tumalofarms.com *** Ingredients . Pasteurized Goats' Milk, Culture, Rennet and Salt."

Class I - Dangerous
Recalled: January 30, 2013 Tumalo Farms Dairy & Eggs

What Should You Do?

  1. Check if you have this product:
    Product is coded with a "born on date" and weight (individual cheese packages are different weight. The product also has a packaged date, which is the same as the ship date. there are 2 born on dates - 1/10/13 and 1/24/13
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Tumalo Farms LLC
Reason for Recall:
Improperly pasteurized.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

A soft chevre-style cheese. Label reads in part, "*** TUMALO FARMS Artisan Cheeses of Central Oregon Chevita This fresh and mild, soft, white cheese has a great tangy finish www.tumalofarms.com *** Ingredients . Pasteurized Goats' Milk, Culture, Rennet and Salt."

Product Codes/Lot Numbers:

Product is coded with a "born on date" and weight (individual cheese packages are different weight. The product also has a packaged date, which is the same as the ship date. there are 2 born on dates - 1/10/13 and 1/24/13

Distribution:

Distributed in: WA, OR

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1000-2013

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