Amish Potato Salad, Formula PO.08, packaged under these labels: -Reser's Fine Foods Amish Potato Salad, packaged in 6/16-oz (UPC 071117190458), 6/3-lb (UPC 071117193169) and 3/8-lb (UPC 071117004380) carton cases. Distributed by Reser's Fine Foods, Beaverton, OR. -Yoder's Amish Potato Salad, Original Recipe, packaged in 6/32-oz (073474010394), 6/3-lb (UPC 073474681631) and 2/5-lb (UPC 073474887286) carton cases. Distributed by Lipari Foods, Warren, MI.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Use by dates 10/23/13-11/26/13.
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- 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:
Amish Potato Salad, Formula PO.08, packaged under these labels: -Reser's Fine Foods Amish Potato Salad, packaged in 6/16-oz (UPC 071117190458), 6/3-lb (UPC 071117193169) and 3/8-lb (UPC 071117004380) carton cases. Distributed by Reser's Fine Foods, Beaverton, OR. -Yoder's Amish Potato Salad, Original Recipe, packaged in 6/32-oz (073474010394), 6/3-lb (UPC 073474681631) and 2/5-lb (UPC 073474887286) carton cases. Distributed by Lipari Foods, Warren, MI.
Product Codes/Lot Numbers:
Use by dates 10/23/13-11/26/13.
Distribution:
Nationwide distribution
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: F-0248-2014
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