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FDA · FoodClass I

Braga Fresh Foods LLC food recall: Marketside

ListeriaMicrobial contamination

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Food
Classification
Class I
Status
Ongoing
Event ID
96081
Recall initiated
Dec 27, 2024
Classified by FDA
Jan 27, 2025
Posted in Enforcement Report
Jan 29, 2025
Recalling firm
Braga Fresh Foods LLC
Firm location
Salinas, CA, United States
Initiated by
Voluntary: Firm initiated
Firm notified customers by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Products in this event
1

What to do

Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.

View the official FDA record ↗

Reason for recall

Potential contamination with Listeria monocytogenes.

What the classification means

  • Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.

About this recall

The firm started this recall on Dec 27, 2024. FDA classified it 31 days later, on Jan 27, 2025. Distribution reported by FDA: Walmart retail stores: AK, AR, AZ, CA, CO, ID, IL, IN, KY, LA, MI, MT, NV, OH, OK, OR, TX, UT, WA, WY Braga Fresh Foods LLC has 4 recalls in our records.

Recalled products (1)

  • F-0424-2025 Class I Ongoing

    Marketside, BROCCOLI FLORETS, 12oz, BEST IF USED BY DEC 10 2024, PRODUCT OF USA, MEXICO

    Codes / lots: BFFG327A6 13:56

    Quantity: 5,918 cases (6x12oz/case)

Source and freshness

Source
U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
Official notice
FDA Enforcement Report, event 96081
Raw record
openFDA API (JSON)
Dataset last updated by FDA
Nov 3, 2026
Imported by RecallRadar
Nov 4, 2026

Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.

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