CLASS IFood recall · Reported 1 Jan 2014 · FDA Enforcement Report
Mustard Potato Salad, Formula PO.57 recalled by Reser's Fine Foods
Reser's Fine Foods is recalling Mustard Potato Salad, Formula PO.57, packaged under these labels: -Reser's Mustard Potato, distributed in 41 states. The recall was initiated on 22 Oct 2013 and the FDA has classified it as Class I.
Check your package
Lot, batch or date codesUse by dates 10/21/13-11/25/13.
Quantity recalledN/A
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
The recalled products are potentially contaminated with Listeria monocytogenes.
Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.
Product as listed by the FDA
Mustard Potato Salad, Formula PO.57, packaged under these labels: -Reser's Mustard Potato Salad, packaged in 12/16-oz (UPC 071117190038 & 071117183344), 6/32-oz (UPC 071117181531 ), 6/3-lb (UPC 071117193039), 3/4-lb (UPC 071117002270 ) and 3/8-lb carton cases. Also Reser's Deli Salads packaged in 6/3-lb carton cases. Distributed by Reser's Fine Foods, Beaverton, OR. -Essentail Everyday Mustard Potato Salad, packaged in 6/16-oz (UPC 041303820162 ) and 6/3-lb (UPC 041303820193) carton cases. Distributed by Supervalu Inc., Eden Prairie, MN. -Cross Valley Farms Potato Salad, packaged in 2/8-lb carton cases. Distributed by U.S. Foodservice, Inc., Rosemont, IL. UPC 758108301597 -King Sooper's Mustard Potato Salad, packaged in 12/1-lb (UPC 071117654752) and 3/4-lb (UPC 071117646405) carton cases. -West Creek Mustard Potato Salad, packaged in 2/5-lb carton cases. Distributed by Performance Food Group, Richmond, VA. UPC 806795286809 -Little Salad Bar Mustard Potato Salad (Aldi brand), packaged in 6/32-oz carton cases. Distributed by ALDI Inc., Batavia, IL. UPC 041498182915
Where it was distributed
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.
The recalled products are potentially contaminated with Listeria monocytogenes.
Which lots are affected?
Use by dates 10/21/13-11/25/13.
Where was it sold?
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.
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.