Check the Batch
Class IITerminated in FDA datasetJul 15, 2015

Italian Vegetable Blend. Product is frozen, not ready to eat, label carries cooking instruction. Label reads in part "***MARKON FIRST CROP*** A proof of the label was provided, it does not…

Recalling firm: National Frozen Foods Corporation--Seattle

Why it was recalled

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

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The exact product

Italian Vegetable Blend. Product is frozen, not ready to eat, label carries cooking instruction. Label reads in part "***MARKON FIRST CROP*** A proof of the label was provided, it does not contain product identity, net wt or ingredients. This product is available in two sizes, 12/2 lb or 20 lb. Copies of case labels were provided. Label reads in part "***20 KB NET WT. 349548 MARKON FIRST CROP ***ITALIAN BLEND CONTAINS: BROCCOLI, CAULIFLOWER, CARROTS, ITALIAN BEANS, LIMA BEANS,***(UPC) 0 07 23234 13245 2***" No UPC on blue liner. Shipping Case UPC Code 10723234132954. "***12/2 lbs 349547 MARKON FIRST CROP***ITALIAN BLEND CONTAINS: BROCCOLI, CAULIFLOWER, CARROTS, ITALIAN BEANS, LIMA BEANS***" No UPC on generic bags; Shipping Case UPC Code 10723234132954.

vegetables

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

Lot Code Information 20 LB - Item # 23234-13245 - 29097-4G02G3N and 30774-5B17M3N,with corresponding expiration dates 7/2/2016 and 2/17/2017. 12/2 lb - Item # 23234-13295 29568-4J18J3N, 29949-4L04D3N, 29949-4L04E3N, 30773-5B17K3N, and 30773-5B17L3N with corresponding expiration dates 9/18/2016, 11/4/2016, 11/4/2016, and 2/17/2017.

Recall details

Recall number
F-0207-2016
Event ID
71731
FDA status
Terminated
Initiated
Jul 15, 2015
Reported
Nov 25, 2015
Classified
Nov 13, 2015
Terminated
Jan 29, 2016
Quantity
1,719 cases or 41,256 lbs
Location
Seattle, WA, 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

distributed nationwide

FDA source record · F-0207-2016

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.