Marketside, BROCCOLI FLORETS, 12oz, BEST IF USED BY DEC 10 2024, PRODUCT OF USA, MEXICO
Summary
The FDA issued a Class I for Marketside, BROCCOLI FLORETS, 12oz, BEST IF USED BY DEC 10 2024, PRODUCT OF USA, by Braga Fresh Foods LLC. Reason: Potential contamination with Listeria monocytogenes..
Details
Source
Food Recall
External ID
F-0424-2025
Action Date
2025-01-29
Status
Ongoing
Category
food
Product Description
Marketside, BROCCOLI FLORETS, 12oz, BEST IF USED BY DEC 10 2024, PRODUCT OF USA, MEXICO
Lot/Code Info: BFFG327A6 13:56
Quantity Affected: 5,918 cases (6x12oz/case)
Reason for Recall
Potential contamination with Listeria monocytogenes.
Distribution
Walmart retail stores: AK, AR, AZ, CA, CO, ID, IL, IN, KY, LA, MI, MT, NV, OH, OK, OR, TX, UT, WA, WY
Type: Voluntary: Firm initiated
Recall Initiated: 2024-12-27
Company
Salinas, 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 36 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Braga Fresh Foods LLC has 2 FDA actions in our database, including 2 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 (Braga Fresh Foods LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Braga Fresh Foods LLC have FDA actions?
Braga Fresh Foods LLC has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0424-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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