Signature Cafe Sandwich Philly Cheesesteak hot and cold;regular and large sizes. All Signature Cafe Made to order sandwiches for which customers asked for optional green Pepper and yellow onion mix. Manufactured by GH Foods CA LLC, Rancho Cordova, CA.

Class I - Dangerous
Recalled: July 26, 2012 GH Foods CA Dairy & Eggs

What Should You Do?

  1. Check if you have this product:
    Reg hot UPC: 21012800000; Reg cold UPC: 21009100000; Large hot UPC: 21012700000; Large cold UPC: 2109900000 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:

Signature Cafe Sandwich Philly Cheesesteak hot and cold;regular and large sizes. All Signature Cafe Made to order sandwiches for which customers asked for optional green Pepper and yellow onion mix. Manufactured by GH Foods CA LLC, Rancho Cordova, CA.

Product Codes/Lot Numbers:

Reg hot UPC: 21012800000; Reg cold UPC: 21009100000; Large hot UPC: 21012700000; Large cold UPC: 2109900000 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-1914-2012

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