Del Monte Research Center - Walnut Creek Recall: Record review found the several productions runs were processed using the incorrect thermal process, and therefore the potential for Clostridium botulinum. - F-0762-2019
🇺🇸 United States
TerminatedClass II
Company
Del Monte Research Center - Walnut Creek
Product
Del Monte Quality Fresh Cut Harvest Selects Fiesta Corn seas…
Recall date
December 11, 2018
Terminated
April 17, 2019
Source
FDA
Reason for recall
Record review found the several productions runs were processed using the incorrect thermal process, and therefore the potential for Clostridium botulinum.
- Recall initiated
- Reported by source
- Recall terminated
Recalled products
Product description
UPC
Quantity
Lot / code information
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
Not published in this source record
64,242 cases
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
Distribution
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.
Official source record
Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0762-2019
Event ID
81768
Status
Terminated
Classification
Class II
Company
Del Monte Research Center - Walnut Creek
Product description
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
Quantity
64,242 cases
Reason
Record review found the several productions runs were processed using the incorrect thermal process, and therefore the potential for Clostridium botulinum.
Recall initiation date
December 11, 2018
Report date
January 30, 2019
Classification date
Not published in this source record
Termination date
April 17, 2019
Distribution pattern
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.
UPC, lot, and code information
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
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
A map highlighting the states named in the source's distribution description.
Distributed
No data published
Shading reflects state-level totals only, as published by the source. It does not imply
county-level or point-level precision.
Distribution map
State
Distributed
Alabama
1
California
1
Connecticut
1
Florida
1
Georgia
1
Illinois
1
Indiana
1
Kansas
1
Louisiana
1
Maryland
1
Michigan
1
Mississippi
1
North Carolina
1
New Jersey
1
New York
1
Oklahoma
1
South Carolina
1
Vermont
1
Virginia
1
Washington
1
Texas
1
Tennessee
1
Wisconsin
1
Arkansas
1
Missouri
1
Ohio
1
Minnesota
1
Iowa
1
Colorado
1
Arizona
1
Delaware
1
New Hampshire
1
Oregon
1
Utah
1
States shown are extracted from the source's free-text distribution description above; a narrative
description (e.g. "distributed nationwide") may not list individual states to extract.
View raw source data
-- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
FDA classifies this recall as Class II. See how to read an FDA recall record (linked above) for what each classification level means.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
Official guidance and record verification
Public Health Trace does not provide medical advice -- review the linked official source below for
current, authoritative information.
How to interpret this historical record
This record is preserved as published by FDA, as of April 17, 2019.
Status as reported: Terminated.
This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company
or product is unsafe beyond what the official source has published.
Read the full medical disclaimer.