FDA recall record

Michael Foods Shell Eggs packaged under the following labels recall — FDA F-0023-2015

Shell eggs contaminated with Pseudomonas fluorescens.

Class IIIclassification
F-0023-2015official record ID
Oct 22, 2014report date

Recall record at a glance

Official recordF-0023-2015
CategoryFood Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmMichael Foods, Inc.
Report dateOct 22, 2014
Recall initiation dateJul 8, 2014
Quantity40,966 cases
LocationMinnetonka, MN, United States

Official product description

Shell Eggs packaged under the following labels: (1) Abbotsford Farms Cage Free Pasteurized Shell Eggs, Grade A Large Brown Eggs, packaged as 15 dozen per 1 case. Distributed by Abbotsford Farms, Gaylord, MN 55334. UPC Code 1 00 14616 64010 7. (2) AbbotsFord Farms Cage Free 1 Dozen Large Eggs Pasteurized for Safety. The product was packaged as 1 case of 15 1-dozen eggs per carton. Distributed by Abbotsford Farms, Gaylord, MN 55334. UPC Code 1 00 14616 64010 6. (3) Pepetti's Pasteurized Shell Eggs made with Grade A Large White Eggs, packaged as 15 dozen per 1 case. Distributed by: Michael Foods, Inc., Minnetonka, MN 55305. UPC Code 1 07 46025 86990 7. (4) Glenview Farms Pasteurized Shell Eggs made with Grade A Large White Eggs, packaged as 15 dozen per 1 case. Distributed by U.S. Foodservice Inc., Rosemount, IL 60018. UPC Code 5 07 58108 62234 5. (5) Crystal Farms One Dozen Large Eggs, Pasteurized Eggs. The product was packaged as 1 case of 15 1-dozen eggs per carton. Distributed by Crystal Farms, Lake Mills, WI 53551-0753. UPC Code 1 00 75925 00032 6. (6) GFS Large Pasteurized Eggs, packaged as 15 dozen per 1 case. Distributed by Gordon Food Service, Grand Rapids, MI 49548. UPC Code 0 00 93901 26545 6.

Why the product was recalled

Shell eggs contaminated with Pseudomonas fluorescens.

Distribution information

Nationwide distribution. No product was distributed to foreign, military, or government facilities.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Telephone.

What to do next

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