CLASS II Food recall · Reported 25 Nov 2015 · FDA Enforcement Report

Italian Vegetable Blend recalled by National Frozen Foods

National Frozen Foods Corporation--Seattle is recalling Italian Vegetable Blend, distributed nationwide in the US. The recall was initiated on 15 Jul 2015 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codes12/2lb - Item # 71179-18875 - LOT #'s 965DEC051403E, 965DEC051403F, 965DEC051403G, 965FEB041503C, 965FEB041503D, 965FEB041503E, 965FEB041503F, 965FEB251503E, 965MAR191504D, 965MAR311503J, 965MAR311503K, 965MAR311503L, 965MAR311503M, 965MAY281503G, 965MAY281503H, 965MAY281503J, and 965MAY281503K with corresponding expiration dates 12/5/2016, 12/5/2016, 12/5/2016, 2/4/2017, 2/4/2017, 2/4/2017 2/4/2017, 2/25/2017, 3/19/2017, 3/31/2017, 3/31/201, 3/31/2017, 3/31/2017, 5/28/2017, 5/28/2017, 5/28/2017, and 5/28/2017. 20lb - Item # 71179-18887 lot # 965DEC051402J, expiration date 12/5/2016.
Quantity recalled215,616 lbs or 8984 cs (12/2lb) and 33140 lbs or 1657 cs (20 lbs)

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0204-2016
FDA event ID
71731
Classification
Class II
Status
Terminated
Recall initiated
15 Jul 2015
FDA classified
13 Nov 2015
Reported
25 Nov 2015
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Listeria
Product category
Ready Meals

Timeline

15 Jul 2015Recall initiated by company
13 Nov 2015Classified by FDA+121 days
25 Nov 2015Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.

Product as listed by the FDA

Italian Vegetable Blend. Product is frozen, not ready to eat, label carries cooking instruction. Label reads in part "***SIMPLOT CLASSIC*** ITALIAN BLEND*** INGREDIENTS: ZUCCHINI, CARROTS, CAULIFLOWER, ITALIAN BEANS, LIMA BEANS, RED BELL PEPPER***" For 12/2 lb UPC on proof for bag 0 71179 18875 2. Shipping Case UPC Code 10071179188759. For 20 lb. case, a blue liner is used (no UPC), Shipping Case UPC Code 10071179188872. 20 LBS. NET WT case consists of one unmarked blue poly bag. 32oz (2 LBS) - case consists of 12/32oz packages Copy of proof for bag and proof for case label provided.

Where it was distributed

distributed nationwide

Nationwide

Questions about this recall

Why was it recalled?

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

Which lots are affected?

12/2lb - Item # 71179-18875 - LOT #'s 965DEC051403E, 965DEC051403F, 965DEC051403G, 965FEB041503C, 965FEB041503D, 965FEB041503E, 965FEB041503F, 965FEB251503E, 965MAR191504D, 965MAR311503J, 965MAR311503K, 965MAR311503L, 965MAR311503M, 965MAY281503G, 965MAY281503H, 965MAY281503J, and 965MAY281503K with corresponding expiration dates 12/5/2016, 12/5/2016, 12/5/2016, 2/4/2017, 2/4/2017, 2/4/2017 2/4/2017, 2/25/2017, 3/19/2017, 3/31/2017, 3/31/201, 3/31/2017, 3/31/2017, 5/28/2017, 5/28/2017, 5/28/2017, and 5/28/2017. 20lb - Item # 71179-18887 lot # 965DEC051402J, expiration date 12/5/2016.

Where was it sold?

distributed nationwide

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

8 other products · FDA event 71731

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