Tomato 3 Count UPC 0 33383 65504 8, 10lb box, 25lb box & 60ct/2 layer box Williams Farms Repack, LLC Lodge, SC 29082
Summary
The FDA issued a Class I for Tomato 3 Count UPC 0 33383 65504 8, 10lb box, 25lb box & 60ct/2 layer box Willia by Williams Farms Produce Sales Co., Inc.. Reason: Product may contain Salmonella..
Details
Source
Food Recall
External ID
F-0822-2025
Action Date
2025-06-04
Status
Ongoing
Category
food
Product Description
Tomato 3 Count UPC 0 33383 65504 8, 10lb box, 25lb box & 60ct/2 layer box Williams Farms Repack, LLC Lodge, SC 29082
Lot/Code Info: Lot R4467 & R4470
Quantity Affected: 50/3 pack tray; 77/10lb box; 673/25lb box; 419/60ct 2 layer box
Reason for Recall
Product may contain Salmonella.
Distribution
Product was shipped to the following states: GA, NC & SC.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-04-30
Company
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 17 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (Williams Farms Produce Sales Co., Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Williams Farms Produce Sales Co., Inc. have FDA actions?
This is the only FDA action we have on record for Williams Farms Produce Sales Co., Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0822-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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