Dole 8oz Shredded Lettuce Product UPC 071430010655 Lidl 8oz Shred Lettuce Product UPC 4056489151272 Little Salad Bar 8oz Shredded Lettuce Product UPC 4099100087963 Dole 8 oz Shredded Lettuce Product UPC 0-71430-01065-5 Marketside 8 oz Shredded Lettuce Product UPC 6-81131-32896-8 Kroger 8oz Shredded Lettuce Product UPC 0-11110-91613-6

Class I - Dangerous
Recalled: December 22, 2021 Dole Fresh Vegetables Produce Nationwide

What Should You Do?

  1. Check if you have this product:
    Code beginning with either the letter "N" or "Y" Y318 thru Y355 all lines Best if Used By date between November 30, 2021 and January 8, 2022
  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:
Dole Fresh Vegetables Inc
Reason for Recall:
Potential 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:

Dole 8oz Shredded Lettuce Product UPC 071430010655 Lidl 8oz Shred Lettuce Product UPC 4056489151272 Little Salad Bar 8oz Shredded Lettuce Product UPC 4099100087963 Dole 8 oz Shredded Lettuce Product UPC 0-71430-01065-5 Marketside 8 oz Shredded Lettuce Product UPC 6-81131-32896-8 Kroger 8oz Shredded Lettuce Product UPC 0-11110-91613-6

Product Codes/Lot Numbers:

Code beginning with either the letter "N" or "Y" Y318 thru Y355 all lines Best if Used By date between November 30, 2021 and January 8, 2022

Distribution:

Nationwide distribution

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0687-2022

Related Recalls