Class ITerminated in FDA datasetOct 22, 2013

Cranberry Orange Relish, Formula GE.14, packaged under the following labels: -Reser's Cranberry Orange Relish packaged in 6/12--oz (

Recalling firm: Reser's Fine Foods, Inc.

Why it was recalled

The recalled products are potentially contaminated with Listeria monocytogenes.

Check your package

Compare the exact product and package details with the label you have.

ProductCranberry Orange Relish, Formula GE.14, packaged under the following labels: -Reser's Cranberry Orange Relish packaged in 6/12--oz (UPC 071117280029) and 2/8-lb (UPC 071117804003) carton cases. Distributed by Reser's Fine Foods, Beaverton, OR. -Yoder's Cranberry Relish packaged in 2/5-lb carton cases. Orval Kent Foods, Wheeling, IL. UPC 073474681143
UPC071117280029, 071117804003, 073474681143

FDA code information

Use by dates 10/22/13 - 12/07/13.

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Cranberry Orange Relish, Formula GE.14, packaged under the following labels: -Reser's Cranberry Orange Relish packaged in 6/12--oz (UPC 071117280029) and 2/8-lb (UPC 071117804003) carton cases. Distributed by Reser's Fine Foods, Beaverton, OR. -Yoder's Cranberry Relish packaged in 2/5-lb carton cases. Orval Kent Foods, Wheeling, IL. UPC 073474681143

Extracted codes and context

TypeCode / valueContext
UPC071117280029following labels: -Reser's Cranberry Orange Relish packaged in 6/12--oz (UPC 071117280029) and 2/8-lb (UPC 071117804003) carton cases. Distributed by Reser's Fine Foods, Beaverton, OR. -Yoder's Cranberry
UPC071117804003Cranberry Orange Relish packaged in 6/12--oz (UPC 071117280029) and 2/8-lb (UPC 071117804003) carton cases. Distributed by Reser's Fine Foods, Beaverton, OR. -Yoder's Cranberry Relish packaged in 2/5-lb cart
UPC073474681143ry Relish packaged in 2/5-lb carton cases. Orval Kent Foods, Wheeling, IL. UPC 073474681143

Recall details

Recall number
F-1181-2014
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.

FDA source record · F-1181-2014

Data updated September 16, 2026. View official FDA data ↗

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