Recall record at a glance
| Official record | F-1195-2014 |
|---|---|
| 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
Elbow Macaroni Salad, Formula MA.22, packaged under the following labels: -West Creek Elbow Macaroni Salad packaged in 2/5-lb carton cases. Distributed by Performance Food Group, Richmond, VA. -Cobblestreet Market Elbow Macaroni Salad packaged in 3/8-lb carton cases. Marketed by Independent Marketing Alliance, Houston, TX. -Essential Everyday Classic Macaroni Salad packaged in 6/16-oz and 6/3-lb carton cases. Distributed by Supervalu Inc., Eden Prairie, MN. -Little Salad Bar Macaroni Salad packaged in 3/32-oz carton cases. Distributed by ALDI Inc., Batavia, IL. -Cross Valley Farms Elbow Macaroni Salad packaged in 2/8-lb carton cases. Distributed by US Foods, Rosemont, IL. -Reser's Elbow Macaroni Salad packaged in 3/8-lb, 3/4-lb, 12/3.5-oz, 6/32-oz, 12/12-oz, 12/454 grams, 12/16-oz, 6/32-oz and 6/3-lb carton cases. Reser's Fine Foods, Inc., Beaverton, OR. -King Soopers City Market Regular Macaroni Salad packaged in 3/4-lb carton cases. Distributed by King Soopers Inc., Denver, CO. -Yoder's Macaroni Salad Original Recipe packaged in 6/32-oz, 6/3-lb, 2/5-lb and 12/16-oz carton cases. Distributed By Lipari Foods, Warren, MI. -Sysco Classic Elbow Macaroni Salad packaged in 3/8-lb carton cases. Distributed By Sysco Corporation, Houston, TX.
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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