FDA recall record

CRF Frozen Foods Frozen Organic Mixed Vegetables, Wellsley Farms Organic brand recall — FDA F-1762-2016

Organic Organic Mixed Vegetables product is recalled due to a potential for contamination with Listeria monocytogenes.

Class Iclassification
F-1762-2016official record ID
Jul 27, 2016report date

Recall record at a glance

Official recordF-1762-2016
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmCRF Frozen Foods, LLC
Report dateJul 27, 2016
Recall initiation dateApr 22, 2016
Quantity6083 cases total
LocationPasco, WA, United States

Official product description

Frozen Organic Mixed Vegetables, Wellsley Farms Organic brand, net wt. 4 lb. The UPC is 8 88670 01013 6. Product label bears cooking instructions and listed as: MICROWAVE 1. Pour one quarter contents of bag into a microwave safe dish with 1/4 cup water. 2. Cook covered on HIGH 3 minutes 3. Stir and continue cooking uncovered for 3 to 4 minutes or until heated through* 4. Season to taste and serve. STOVE TOP 1. Pour one quarter contents of bag into saucepan with 1/2 cup water. 2. Heat to a boil over medium -high heat. 3. Stir, reduce heat to simmer and cover. 4. Maintain simmer, stirring occasionally, 10 to 12 minutes or until heated through* 5. Season to taste and serve * For food safety and best product quality cook to a temperature of 160F. Since microwave ovens may vary in power, these instructions are guidelines only. Do not refreeze after thawing.

Why the product was recalled

Organic Organic Mixed Vegetables product is recalled due to a potential for contamination with Listeria monocytogenes.

Distribution information

distributed in AL, AZ, CA, CO, CT, DE, FL, GA, ID, IL, IN, LA, MD, MA, MI, MN, MO, MT, NV, NH, NJ, NY, NC, OH, OR, PA, RI, SC, TN, UT, VT, VA, WA, WV, WI, and in British Columbia, Alberta, Manitoba, Saskatchewan of Canada.

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

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