Class IITerminated in FDA datasetOct 22, 2013

Krab Dip, Formula PT.152 packaged under these labels: -Reser's Cajun Krab Dip packaged in 2/5-lb (

Recalling firm: Reser's Fine Foods, Inc.

Why it was recalled

The recalled products are potentially contaminated with Listeria monocytogenes.

Check the codes ↓

The exact product

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.

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 10/20/13 - 12/04/13.

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

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 ↗

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.