Vegetable products including: BROCCOLI FLORETS 3 LB BROCCOLI FLORETS LB BROCCOLI FLORETS PLU 4548 PRE-PACKAGED BROCCOLI FLORETS BROCCOLI FLORETS 3 LB BAG

Class I - Dangerous
Recalled: October 20, 2017 Meijer Distribution Produce

What Should You Do?

  1. Check if you have this product:
    Items purchased September 27, 2017 through October 20, 2017, the following UPC Codes: 0-0-4548-3, 0-72668-20001-6, 2-21234-00000-4, 7-16519-01015-6, UPC: 22952300000, Best By Date / Julian Code 10/14/17 - 271 10/16/17 - 273 10/18/17 - 275 10/19/17 - 276
  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:
Meijer Distribution, Inc
Reason for Recall:
Meijer Inc. is voluntarily recalling multiple processed vegetable products following a supplier's recall due to potential contamination 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:

Vegetable products including: BROCCOLI FLORETS 3 LB BROCCOLI FLORETS LB BROCCOLI FLORETS PLU 4548 PRE-PACKAGED BROCCOLI FLORETS BROCCOLI FLORETS 3 LB BAG

Product Codes/Lot Numbers:

Items purchased September 27, 2017 through October 20, 2017, the following UPC Codes: 0-0-4548-3, 0-72668-20001-6, 2-21234-00000-4, 7-16519-01015-6, UPC: 22952300000, Best By Date / Julian Code 10/14/17 - 271 10/16/17 - 273 10/18/17 - 275 10/19/17 - 276

Distribution:

Distributed in: IL, IN, KY, MI, OH, WI, VA

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0246-2018

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