Potato Salad, Formula PO.70, packaged under these labels: -Reser's Fine Fo...
FDA Recall #F-0236-2014 — Class I — October 22, 2013
Recall Summary
| Recall Number | F-0236-2014 |
| Date Initiated | October 22, 2013 |
| Classification | Class I |
| Status | Terminated |
| Type | Voluntary: Firm initiated |
| Product Type | Food |
Recalling Firm
| Firm | Reser's Fine Foods, Inc. |
| Location | Beaverton, OR |
Product Description
Potato Salad, Formula PO.70, packaged under these labels: -Reser's Fine Foods, Original Potato Salad, in 12/12-oz (UPC 071117182200), 6/32-oz (UPC 071117181500), 3/4-lb (UPC 071117002232), 3/8-lb (UPC 071117002157), 12/3.5-oz (UPC 071117170009), 12/5.5-oz (UPC 071117171006) and 2/10-lb (UPC 071117002782) container cases. Also distributed in a 6/4-lb party pack (UPC 071117001624). Distributed by: Reser's Fine-Foods, Beaverton, OR. -Yoder's American Potato Salad, in 6/32-oz (UPC 073474010462), 2/5-lb (UPC 073474550098), 6/3-lb (UPC 073474010219) and 12/16-oz (UPC 073474887385) carton cases. -West Creek, Original Potato Salad, in 2/5-lb carton cases. (UPC 806795286793) Distributed by Performance Food Group, Richmond, VA. -Essential Everday Original Potato Salad packaged in 6/16-oz (UPC 041303820131) and 6/3-lb (UPC 041303820209) carton cases. Distributed by Supervalu Inc., Eden Prairie, MN. -7-11 Potato Salad, in 12/7-oz carton cases. (UPC 052548517526) Distributed by 7-Eleven, Inc., Dallas, TX. -Cross Valley Farms Family Style Potato Salad packaged in 2/8-lb carton cases. Distributed by US Foodservice, Inc., Rosemont, IL. UPC 758108373877 -Sysco Classic Potato Salad, in 3/8-lb carton cases. (UPC 074865100915)
Reason for Recall
The recalled products are potentially contaminated with Listeria monocytogenes.
Classification
Class I — A situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.
Distribution Pattern
Distribution was made to AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MO, MS, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, VA, WI, WV AND WY. Distribution was also made to Canada.
Product Quantity
N/A
Product Codes / Lot Numbers
Use by date 10/13/2013 - 11/15/13.
What Should You Do?
Stop consuming this product immediately. Check your home for the recalled item and dispose of it safely. If you experienced a health issue after consuming this product, contact your doctor and report it to the FDA MedWatch.
Frequently Asked Questions
Stop consuming the product immediately and do not donate or give it to others. Check the recall notice above for specific disposal or return instructions. Many food recalls ask you to throw the product away and retain the packaging for a possible refund from the retailer. If you purchased it online, check your order history — some retailers send recall notifications directly to customers. You do not need a receipt to report an issue or seek a refund; the fact of purchase is typically sufficient.
Listeria monocytogenes is one of the most serious foodborne pathogens. Unlike most bacteria, Listeria can grow at refrigerator temperatures (below 40°F), meaning refrigerating a contaminated product does not stop the risk. Symptoms can appear 1 to 4 weeks after eating contaminated food and may include fever, muscle aches, headache, stiff neck, confusion, and loss of balance. Listeriosis is particularly dangerous for pregnant women — infection can cause miscarriage, stillbirth, or premature delivery. If you consumed this recalled product and are in a high-risk group (pregnant, elderly, or immunocompromised), contact your doctor immediately even if you feel well.
Report foodborne illnesses and adverse food reactions to the FDA through the MedWatch Safety Reporting Portal at FDA.gov, or by calling 1-800-332-1088. You can also report issues directly to the FDA's Safety Reporting Portal at SafetyReporting.hhs.gov. If you believe there is an immediate public health risk, contact your local health department. Your report helps the FDA identify contamination patterns, initiate recalls faster, and protect other consumers from the same hazard. Include as much detail as possible: the product name, lot code, purchase date and location, and a description of your symptoms or findings.
The FDA assigns a status to each recall action throughout its lifecycle. "Ongoing" means the recall is active — the firm is still working to remove the product from commerce and notify consumers. "Completed" means the recall strategy has been implemented and the FDA has determined that the recalling firm has taken all appropriate steps to remove the product. "Terminated" means the FDA has reviewed the results and concluded the recall is complete. Even if a recall is marked as completed or terminated, you should still discard any recalled products you find at home — the recall status refers to the firm's compliance actions, not the safety of product still in consumers' possession.