Recall record at a glance
| Official record | F-0250-2014 |
|---|---|
| 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
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
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
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.