🔍 RecallPedia

Kentucky Bleu cheese was sold in the Louisville, KY, Whole Foods Market store, and was cut and packaged in clear plastic wrap. It was sold with a Whole Foods Market scale label reading 'Kenny's Farmhouse Cheese KY BL".

Class I - Dangerous
🍎 Food Recalled: October 5, 2012 Whole Foods Market Brand 365 Dairy & Eggs

What Should You Do?

  1. Check if you have this product:
    The "Kenny's Farmhouse Cheese KY BL" has a PLU of 209578 and includes all 'sell by' dates, which are noted on the scale label.
  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:
Whole Foods Market Brand 365, Llc
Reason for Recall:
Whole Foods Market announces that it is recalling "Kenny's Farmhouse Cheese KY BL" sold in its Louisville, KY store and "Blue Kentucky Rose Kenny's" cheese sold in its Nashville, TN store. These cheeses are being recalled because they have the potentia
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Kentucky Bleu cheese was sold in the Louisville, KY, Whole Foods Market store, and was cut and packaged in clear plastic wrap. It was sold with a Whole Foods Market scale label reading 'Kenny's Farmhouse Cheese KY BL".

Product Codes/Lot Numbers:

The "Kenny's Farmhouse Cheese KY BL" has a PLU of 209578 and includes all 'sell by' dates, which are noted on the scale label.

Distribution:

Distributed in: KY

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0868-2013

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