Summary
The FDA issued a Class I for Marketside Southwest Chopped Kit 10.3 oz. UPC 681131305129 by Ready Pac Foods Inc. Reason: Product has the potential to be contaminated with Listeria monocytogenes..
Details
Source
Food Recall
External ID
F-1004-2024
Action Date
2024-03-06
Status
Terminated
Category
food
Product Description
Marketside Southwest Chopped Kit 10.3 oz. UPC 681131305129
Lot/Code Info: Use by date 12/27/2023 - 1/14/2024 Lot Numbers: 257468982, 257472922, 257474446, 257477419, 257480027, 257481674, 257484256, 257485619
Quantity Affected: 2617 cases
Reason for Recall
Product has the potential to be contaminated with Listeria monocytogenes.
Distribution
U.S. distribution to the following: CA, AZ, WY, NM, HI, CO, CT, DE, MA, MD, ME, MT, NH, NJ, NM, NV, NY, PA, RI, SD, TX, VT, WY
Type: Voluntary: Firm initiated
Recall Initiated: 2024-02-08
Company
Irwindale, 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 128 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Ready Pac Foods Inc has 4 FDA actions in our database, including 4 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 (Ready Pac Foods Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Ready Pac Foods Inc have FDA actions?
Ready Pac Foods Inc has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1004-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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