Kroger Peas & Carrots, Net Wt. 12 oz (340g), UPC 11110-89741; Harris Teeter Peas and Diced Carrots 12 oz, UPC 007203671661

Class I - Dangerous
Recalled: February 17, 2017 Lakeside Foods Other Foods

What Should You Do?

  1. Check if you have this product:
    Kroger Peas & Carrots-Package code: DC*7013 (*Most packages will have a 2 in that space.) Production code: DCMA1127, DCMA1137 BEST BY 01/2019; Harris Teeter Peas and Diced Carrots - Package code: DC*7013 (* Most packages will have a 2 in that space.) Production code: DCMA1127, DCMA1137, Best By: BEST BY 01/2019
  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:
Lakeside Foods, Inc
Reason for Recall:
Lakeside Foods is voluntarily recalling frozen green beans, peas and peas/carrots due to 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:

Kroger Peas & Carrots, Net Wt. 12 oz (340g), UPC 11110-89741; Harris Teeter Peas and Diced Carrots 12 oz, UPC 007203671661

Product Codes/Lot Numbers:

Kroger Peas & Carrots-Package code: DC*7013 (*Most packages will have a 2 in that space.) Production code: DCMA1127, DCMA1137 BEST BY 01/2019; Harris Teeter Peas and Diced Carrots - Package code: DC*7013 (* Most packages will have a 2 in that space.) Production code: DCMA1127, DCMA1137, Best By: BEST BY 01/2019

Distribution:

Distributed in: IN, NC

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1690-2017

Related Recalls