🔍 RecallPedia

MILTON CREAMERY PRAIRIE BREEZE Pasteurized Cow's Milk, Cultures, Salt, Veg.Rennet www.miltoncreamery.com 641-656-4094 Carton Label (not available to consumers) ITEM ID: 02074704 PARIS BROTHERS, INC 8800 NE UNDERGROUND DR KANSAS CITY, MO 64161 (816) 455-4189 MILTON PRAIRIE BREEZE 1 PC 10 LB AVG ITEM ID: 02074701 PARIS BROTHERS, INC 8800 NE UNDERGROUND DR KANSAS CITY, MO 64161 (816) 455-4189 MILTON PRAIRIE BREEZE 1 PC 10 LB RW

Class I - Dangerous
Recalled: May 24, 2022 Paris Brothers Dairy & Eggs

What Should You Do?

  1. Check if you have this product:
    Lot:05062022 Sell By Date: 05/06/2023 or Sell By Date: 03/02/2023
  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:
Paris Brothers Inc
Reason for Recall:
Environmental samples positive for Listeria.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

MILTON CREAMERY PRAIRIE BREEZE Pasteurized Cow's Milk, Cultures, Salt, Veg.Rennet www.miltoncreamery.com 641-656-4094 Carton Label (not available to consumers) ITEM ID: 02074704 PARIS BROTHERS, INC 8800 NE UNDERGROUND DR KANSAS CITY, MO 64161 (816) 455-4189 MILTON PRAIRIE BREEZE 1 PC 10 LB AVG ITEM ID: 02074701 PARIS BROTHERS, INC 8800 NE UNDERGROUND DR KANSAS CITY, MO 64161 (816) 455-4189 MILTON PRAIRIE BREEZE 1 PC 10 LB RW

Product Codes/Lot Numbers:

Lot:05062022 Sell By Date: 05/06/2023 or Sell By Date: 03/02/2023

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1422-2022

Related Recalls