CLASS II Food recall · Reported 30 Jan 2019 · FDA Enforcement Report

Del Monte Quality Fresh Cut Harvest Selects Fiesta Corn recalled

Del Monte Research Center - Walnut Creek is recalling Del Monte Quality Fresh Cut Harvest Selects Fiesta Corn seasoned with Red & Green Peppers, distributed in 34 states. The recall was initiated on 11 Dec 2018 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesBest if Used By dates: " August 14, 2021 " August 15, 2021 " August 16, 2021 " Sept 3, 2021 " Sept 4, 2021 " Sept 5, 2021 " Sept 6, 2021 " Sept 22, 2021 " Sept 23, 2021
Quantity recalled64,242 cases

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-0762-2019
FDA event ID
81768
Recalling firm
Del Monte Research Center - Walnut Creek, Walnut Creek, CA
Classification
Class II
Status
Terminated
Recall initiated
11 Dec 2018
FDA classified
28 Jan 2019
Reported
30 Jan 2019
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Botulism
Product category
Peppers

Timeline

11 Dec 2018Recall initiated by company
28 Jan 2019Classified by FDA+48 days
30 Jan 2019Published in enforcement report+2 days

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

Reason for recall

Record review found the several productions runs were processed using the incorrect thermal process, and therefore the potential for Clostridium botulinum.

Product as listed by the FDA

Del Monte Quality Fresh Cut Harvest Selects Fiesta Corn seasoned with Red & Green Peppers. NET WT 15.25 oz. (432 g); UPC 0 24000 02770; Ingredient: Vegetables (corn, red and green peppers) water, sea salt. Distributed by Del Monte Foods, Walnut Creek, CA 94598

Where it was distributed

U.S. distribution to the following: AL, CA, CT FL, GA, IL, IN, KS, LA, MD, MI, MS, NC, NJ, NY, OK, PN, SC, VT, VA, WA, TX, TN, WI, AR, MO, FL, OH, MO, MN, IA, CO, AZ, AR, DE, NH, OR, UT, Foreign distribution to the following: Bahamas, Barbados, Belize, Bermuda, El Salvador, Haiti, Guyana, Peru, Colombia and Ecuador Uruguay, Aruba, Panama, Saint Lucia, and Suriname.

AlabamaArkansasArizonaCaliforniaColoradoConnecticutDelawareFloridaGeorgiaIowaIllinoisIndianaKansasLouisianaMarylandMichiganMinnesotaMissouriMississippiNorth Carolina

Questions about this recall

Why was it recalled?

Record review found the several productions runs were processed using the incorrect thermal process, and therefore the potential for Clostridium botulinum.

Which lots are affected?

Best if Used By dates: " August 14, 2021 " August 15, 2021 " August 16, 2021 " Sept 3, 2021 " Sept 4, 2021 " Sept 5, 2021 " Sept 6, 2021 " Sept 22, 2021 " Sept 23, 2021

Where was it sold?

U.S. distribution to the following: AL, CA, CT FL, GA, IL, IN, KS, LA, MD, MI, MS, NC, NJ, NY, OK, PN, SC, VT, VA, WA, TX, TN, WI, AR, MO, FL, OH, MO, MN, IA, CO, AZ, AR, DE, NH, OR, UT, Foreign distribution to the following: Bahamas, Barbados, Belize, Bermuda, El Salvador, Haiti, Guyana, Peru, Colombia and Ecuador Uruguay, Aruba, Panama, Saint Lucia, and Suriname.

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

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