Amish Macaroni Salad, Formula MA.8 packaged under the following labels: -Reser's Amish Macaroni packaged in 3/8-lb (
Recalling firm: Reser's Fine Foods, Inc.
Why it was recalled
The recalled products are potentially contaminated with Listeria monocytogenes.
The exact product
Amish Macaroni Salad, Formula MA.8 packaged under the following labels: -Reser's Amish Macaroni packaged in 3/8-lb (UPC 071117004410), 6/16-oz (UPC 071117190441) and 6/3-lb (UPC 071117193152) carton cases. Reser's Fine Foods, Inc., Beaverton, OR. -Yoder's Amish Macaroni Salad in 6/32-oz (UPC 073474010455) and 2/5-lb (UPC 073474887293) carton cases. Distributed by Lipari Foods, Warren, MI.
Check the codes
Compare these FDA-provided codes, lot numbers or dates with the product you have.
Match the product, size and code together. A similar name alone does not identify your batch.
Original FDA code information
Use by dates 10/23/13 - 12/10/13.
| Type | Code / value | Context |
|---|---|---|
| UPC | 071117004410 | under the following labels: -Reser's Amish Macaroni packaged in 3/8-lb (UPC 071117004410), 6/16-oz (UPC 071117190441) and 6/3-lb (UPC 071117193152) carton cases. Reser's Fine Foods, Inc., Beaverton, OR. - |
| UPC | 071117190441 | -Reser's Amish Macaroni packaged in 3/8-lb (UPC 071117004410), 6/16-oz (UPC 071117190441) and 6/3-lb (UPC 071117193152) carton cases. Reser's Fine Foods, Inc., Beaverton, OR. -Yoder's Amish Macaroni Salad |
| UPC | 071117193152 | ckaged in 3/8-lb (UPC 071117004410), 6/16-oz (UPC 071117190441) and 6/3-lb (UPC 071117193152) carton cases. Reser's Fine Foods, Inc., Beaverton, OR. -Yoder's Amish Macaroni Salad in 6/32-oz (UPC 073474010455) |
| UPC | 073474010455 | ne Foods, Inc., Beaverton, OR. -Yoder's Amish Macaroni Salad in 6/32-oz (UPC 073474010455) and 2/5-lb (UPC 073474887293) carton cases. Distributed by Lipari Foods, Warren, MI. |
| UPC | 073474887293 | -Yoder's Amish Macaroni Salad in 6/32-oz (UPC 073474010455) and 2/5-lb (UPC 073474887293) carton cases. Distributed by Lipari Foods, Warren, MI. |
Recall details
- Recall number
- F-1200-2014
- Event ID
- 66563
- FDA status
- Terminated
- Initiated
- Oct 22, 2013
- Reported
- Jan 1, 2014
- Classified
- Dec 24, 2013
- Terminated
- Jan 24, 2017
- Quantity
- N/A
- Location
- Beaverton, OR, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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.
Data updated September 16, 2026. View official FDA data ↗
A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.