Explorateur French Triple Cr¿me cheese (under the names Explorateur, Explorateur French Triple Cr¿me Cheese and Explorateur Triple Cr¿me French Cheese) which were both cut and packaged in clear plastic wrap, as well as sold in branded 8 oz. packages

Class I - Dangerous
Recalled: April 9, 2018 Whole Foods Market Dairy & Eggs

What Should You Do?

  1. Check if you have this product:
    8 ounce packages include the codes: UPC codes 339001000408 and lot codes H10, H010, H11 or H011. The sliced packages include the codes: PLU code 0294317, 203971, 293693 Sell by dates of 02/15/2018-04/03/2018
  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
Reason for Recall:
The cheese has the potential to be contaminated with Listeria monocytogenes.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Explorateur French Triple Cr¿me cheese (under the names Explorateur, Explorateur French Triple Cr¿me Cheese and Explorateur Triple Cr¿me French Cheese) which were both cut and packaged in clear plastic wrap, as well as sold in branded 8 oz. packages

Product Codes/Lot Numbers:

8 ounce packages include the codes: UPC codes 339001000408 and lot codes H10, H010, H11 or H011. The sliced packages include the codes: PLU code 0294317, 203971, 293693 Sell by dates of 02/15/2018-04/03/2018

Distribution:

Distributed in: CT, NJ, IL, NM, TX, AR

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1457-2018

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