Recall record at a glance
| Official record | F-0236-2014 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Reser's Fine Foods, Inc. |
| Report date | Jan 1, 2014 |
| Recall initiation date | Oct 22, 2013 |
| Quantity | N/A |
| Location | Beaverton, OR, United States |
Official 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)
Why the product was recalled
The recalled products are potentially contaminated with Listeria monocytogenes.
Distribution information
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.
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
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