FDA recall record

National Frozen Foods Corporation--Seattle Italian Vegetable Blend recall — FDA F-0206-2016

Italian Vegetable Blend product is recalled due to potential to be contaminated with Listeria monocytogenes.

Class IIclassification
F-0206-2016official record ID
Nov 25, 2015report date

Recall record at a glance

Official recordF-0206-2016
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmNational Frozen Foods Corporation--Seattle
Report dateNov 25, 2015
Recall initiation dateJul 15, 2015
QuantityMonarch 72,696 lbs or 3,029 cs (6/4lb); Valmont 874 cases or 20,904 lbs
LocationSeattle, WA, United States

Official product description

Italian Vegetable Blend. Product is frozen, not ready to eat, label carries cooking instruction. Label reads in part Item # 58108-03475 "***MONARCH***ITALIAN VEGETABLE BLEND CONTAINS ZUCCHINI, CARROTS, CAULIFLOWER, LIMA BEANS AND ITALIAN GREEN BEANS***NET WT***64 OZ***(UPC) 7 58108 03475 4***" Copy of photo of bag label provided. Product is packaged as 6/4 lb bags. Shipping Case UPC Code 5075808034759. Item # 72608-13991 "***12/2 LBS***72608***13991***VALAMONT ITALIAN BLEND CONTAINS: ZUCCHINI, CARROTS, CAULIFLOWER, LIMA BEANS, ITALIAN BEANS***" Shipping UPC Case Code 1 00 72608 13991 5. Copy of case label provided.

Why the product was recalled

Italian Vegetable Blend product is recalled due to potential to be contaminated with Listeria monocytogenes.

Distribution information

distributed nationwide

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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