-Reser's Pumpkin Mousse Dessert, Formula SE.71 packaged in 2/6-lb (
Recalling firm: Reser's Fine Foods, Inc.
Why it was recalled
The recalled products are potentially contaminated with Listeria monocytogenes.
The exact product
-Reser's Pumpkin Mousse Dessert, Formula SE.71 packaged in 2/6-lb (UPC 071117157697) and 6/12-oz (UPC 071117182736) carton cases UPC 071117001518. Reser's Fine Foods, Inc., Beaverton, OR.
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 12/11/13 - 12/30/13.
| Type | Code / value | Context |
|---|---|---|
| UPC | 071117001518 | ed in 2/6-lb (UPC 071117157697) and 6/12-oz (UPC 071117182736) carton cases UPC 071117001518. Reser's Fine Foods, Inc., Beaverton, OR. |
| UPC | 071117157697 | -Reser's Pumpkin Mousse Dessert, Formula SE.71 packaged in 2/6-lb (UPC 071117157697) and 6/12-oz (UPC 071117182736) carton cases UPC 071117001518. Reser's Fine Foods, Inc., Beaverton, OR. |
| UPC | 071117182736 | e Dessert, Formula SE.71 packaged in 2/6-lb (UPC 071117157697) and 6/12-oz (UPC 071117182736) carton cases UPC 071117001518. Reser's Fine Foods, Inc., Beaverton, OR. |
Recall details
- Recall number
- F-1226-2014
- 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.