Seasoned Squash, Onion & Dill sold under the following brand names and package sizes: Albertson's - 10.5 oz Chefs Essentials - 10.5 oz; Raley's - 10.5 oz. Safeway Farms - 10. 5 oz and Manufactured by GH Foods CA LLC, Rancho Cordova, CA.

Class I - Dangerous
Recalled: July 26, 2012 GH Foods CA Other Foods

What Should You Do?

  1. Check if you have this product:
    Albertson's UPC: 8 26766 7900607; Garden Highway UPC's; 7 oz. 8 26766 71120 8; Raley's UPC: 7 oz: 0 46567 71752.4 All with best if Sold by dates of 7/19/12 to 7/31/12.
  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:
GH Foods CA LLC
Reason for Recall:
GH Foods CA received notification from Gills onions of a recall of onions due to Listeria Monocytogenes. GH Foods used the recalled onions in numerous product.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Seasoned Squash, Onion & Dill sold under the following brand names and package sizes: Albertson's - 10.5 oz Chefs Essentials - 10.5 oz; Raley's - 10.5 oz. Safeway Farms - 10. 5 oz and Manufactured by GH Foods CA LLC, Rancho Cordova, CA.

Product Codes/Lot Numbers:

Albertson's UPC: 8 26766 7900607; Garden Highway UPC's; 7 oz. 8 26766 71120 8; Raley's UPC: 7 oz: 0 46567 71752.4 All with best if Sold by dates of 7/19/12 to 7/31/12.

Distribution:

Distributed in: CA, NV, AZ, UT, CO, NM, SD, WY, NE

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1889-2012

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