Dole 9.1oz Peppercorn Ranch Chopped Kit Product UPC 071430000939
Summary
The FDA issued a Class I for Dole 9.1oz Peppercorn Ranch Chopped Kit Product UPC 071430000939 by Dole Fresh Vegetables Inc. Reason: Potential Listeria monocytogenes.
Details
Source
Food Recall
External ID
F-0689-2022
Action Date
2022-02-16
Status
Terminated
Category
food
Product Description
Dole 9.1oz Peppercorn Ranch Chopped Kit Product UPC 071430000939
Lot/Code Info: Code beginning with either the letter "N" or "Y" Best if Used By date between November 30, 2021 and January 8, 2022
Quantity Affected: Total: 207,624 cases from Yuma and 2,081,894 cases from Bessemer City
Reason for Recall
Potential Listeria monocytogenes
Distribution
AL, AZ, CA, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, ND, NE, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI.
Type: Voluntary: Firm initiated
Recall Initiated: 2021-12-22
Company
Monterey, CA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 115 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Dole Fresh Vegetables Inc has 160 FDA actions in our database, including 160 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Dole Fresh Vegetables Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Dole Fresh Vegetables Inc have FDA actions?
Dole Fresh Vegetables Inc has 160 FDA actions in our database, including 160 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0689-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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