🔍 RecallPedia

Kroger (QFC and Fred Meyer) brand, VEGETABLE MEDLEY KFK, Net wt. 10 oz, UPC 8 2676618505 4. Kroger Main & Vine brand, VEGETABLE MEDLEY, Net wt. 10 oz, UPC 8 2676618749 2. Mary's Harvest brand, Rainbow Veggies, 6/24 oz. packages, UPC 0 9250438263 8. Mary's Harvest brand, Veggie Medley Bag, 6/20 oz packages, UPC 0 9250470230 6. Ingredients: Broccoli, Cauliflower, and Carrots.

Class I - Dangerous
Recalled: August 3, 2017 Mary's Harvest Fresh Foods Produce

What Should You Do?

  1. Check if you have this product:
    Use by: 8/5/17 8/8/17. Use by: 8/10/17 8/12/17. Use by: 8/9/17 8/10/17.
  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:
Mary's Harvest Fresh Foods, Inc.
Reason for Recall:
Product is recalled due to potential contamination with E.coli O26.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Kroger (QFC and Fred Meyer) brand, VEGETABLE MEDLEY KFK, Net wt. 10 oz, UPC 8 2676618505 4. Kroger Main & Vine brand, VEGETABLE MEDLEY, Net wt. 10 oz, UPC 8 2676618749 2. Mary's Harvest brand, Rainbow Veggies, 6/24 oz. packages, UPC 0 9250438263 8. Mary's Harvest brand, Veggie Medley Bag, 6/20 oz packages, UPC 0 9250470230 6. Ingredients: Broccoli, Cauliflower, and Carrots.

Product Codes/Lot Numbers:

Use by: 8/5/17 8/8/17. Use by: 8/10/17 8/12/17. Use by: 8/9/17 8/10/17.

Distribution:

Distributed in: OR, WA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-3418-2017

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