Red Potato Salad, Formula PO.62, packaged under the following labels: -Cross Valley Farms Red Royal Potato Salad packaged in 2/8-lb carton cases. Distributed by U.S. Foodservice, Inc., Rosemont, IL. -Reser's Deluxe Red Skin Potato Salad packaged in 2/8-lb carton cases. Reser's Fine Foods, Inc., Beaverton, OR. -Block & Barrel Deluxe Red Skinned Potato Salad packaged in 2/5-lb carton cases. Distributed by Sysco Corporation, Houston, TX.

Class I - Dangerous
Recalled: October 22, 2013 Reser's Fine Foods Baby Food & Formula Nationwide

What Should You Do?

  1. Check if you have this product:
    Use by dates 10/10/13-11/29/13.
  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:
Reser's Fine Foods, Inc.
Reason for Recall:
The recalled products are potentially 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:

Red Potato Salad, Formula PO.62, packaged under the following labels: -Cross Valley Farms Red Royal Potato Salad packaged in 2/8-lb carton cases. Distributed by U.S. Foodservice, Inc., Rosemont, IL. -Reser's Deluxe Red Skin Potato Salad packaged in 2/8-lb carton cases. Reser's Fine Foods, Inc., Beaverton, OR. -Block & Barrel Deluxe Red Skinned Potato Salad packaged in 2/5-lb carton cases. Distributed by Sysco Corporation, Houston, TX.

Product Codes/Lot Numbers:

Use by dates 10/10/13-11/29/13.

Distribution:

Nationwide distribution

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0300-2014

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