Marketside brand celery stick. Net wt. 1.6 OZ. (45g); Rear panel: 1 serving per container; Distributed by Wal-Mart Store
Summary
The FDA issued a Class I for Marketside brand celery stick. Net wt. 1.6 OZ. (45g); Rear panel: 1 serving per by Duda Farm Fresh Foods, Inc.. Reason: Product tested positive for Listeria Monocytogenes..
Details
Source
Food Recall
External ID
F-0706-2025
Action Date
2025-04-23
Status
Terminated
Category
food
Product Description
Marketside brand celery stick. Net wt. 1.6 OZ. (45g); Rear panel: 1 serving per container; Distributed by Wal-Mart Stores, Inc. Bentonville, AR 72716 UPC# 6 81131 16151 0
Lot/Code Info: Best By: 03/23/2025
Quantity Affected: 1,587 cases
Reason for Recall
Product tested positive for Listeria Monocytogenes.
Distribution
Nationwide, PA, GA, TN, MO, IN, TX, NC, KY, FL, VA, OH, IL, WY, CA
Type: Voluntary: Firm initiated
Recall Initiated: 2025-04-04
Company
Oxnard, 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 25 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 (Duda Farm Fresh 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 Duda Farm Fresh Foods, Inc. have FDA actions?
This is the only FDA action we have on record for Duda Farm Fresh Foods, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0706-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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