Gills Onions were used in this product. The Thousand Island Potato Salad is sold at the chef's case, self serve counter, or packaged.It is also sold as "Family Sized Savings Thousand Island Potato Salad". Packaged product is labeled as listed below: "***WHOLE FOODS MARKET***THOUSAND ISLAND POTATO SALAD***POTATOES, CAGE-FREE HARD COOKED EGGS (EGGS, WATER, CITRIC ACID), THOUSAND ISLAND DRESSING....***"

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    None
  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:
Ron Stockman Whole Foods
Reason for Recall:
Whole Foods Market in Florida recalled certain fresh food items sold in the prepared foods department and one item in the seafood department as they could of been made using raw yellow onions processed by Gill Onions, LLC. Gill Onions, LLC initiated a recall on their product due to possible Listeria monocytogenes contamination.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Gills Onions were used in this product. The Thousand Island Potato Salad is sold at the chef's case, self serve counter, or packaged.It is also sold as "Family Sized Savings Thousand Island Potato Salad". Packaged product is labeled as listed below: "***WHOLE FOODS MARKET***THOUSAND ISLAND POTATO SALAD***POTATOES, CAGE-FREE HARD COOKED EGGS (EGGS, WATER, CITRIC ACID), THOUSAND ISLAND DRESSING....***"

Product Codes/Lot Numbers:

None

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-2139-2012

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