Check the Batch
Class IITerminated in FDA datasetRecall initiated Oct 22, 2013

Krab Dip, Formula PT.152 packaged under these labels: -Reser's Cajun Krab Dip packaged in…

Recalling firm: Reser's Fine Foods, Inc.

Why it was recalled

The recalled products are potentially contaminated with Listeria monocytogenes.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jan 24, 2017.

Check your package

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

ProductKrab Dip, Formula PT.152 packaged under these labels: -Reser's Cajun Krab Dip packaged in 2/5-lb (UPC 071117169010) carton cases. Reser's Fine Foods, Inc., Beaverton, OR. -Safeway Cajun Krab Dip packaged in 6/7-oz (UPC 021130124183) carton cases. Reser's Fine Foods, Inc., Beaverton, OR.
UPC021130124183, 071117169010

FDA code information

Use by dates 10/20/13 - 12/04/13.

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

Full FDA record and distribution details

Original product description

Krab Dip, Formula PT.152 packaged under these labels: -Reser's Cajun Krab Dip packaged in 2/5-lb (UPC 071117169010) carton cases. Reser's Fine Foods, Inc., Beaverton, OR. -Safeway Cajun Krab Dip packaged in 6/7-oz (UPC 021130124183) carton cases. Reser's Fine Foods, Inc., Beaverton, OR.

Extracted codes and context

TypeCode / valueContext
UPC021130124183ods, Inc., Beaverton, OR. -Safeway Cajun Krab Dip packaged in 6/7-oz (UPC 021130124183) carton cases. Reser's Fine Foods, Inc., Beaverton, OR.
UPC071117169010packaged under these labels: -Reser's Cajun Krab Dip packaged in 2/5-lb (UPC 071117169010) carton cases. Reser's Fine Foods, Inc., Beaverton, OR. -Safeway Cajun Krab Dip packaged in 6/7-oz (UPC 021130124

Original FDA recall reason

The recalled products are potentially contaminated with Listeria monocytogenes.

Recall details

Recall number
F-1209-2014
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-1209-2014

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

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