Loaded Veggie Grain Bowl; Net Wt. 10.90 Oz (309g) GTIN code: 00818905028162
Summary
The FDA issued a Class II for Loaded Veggie Grain Bowl; Net Wt. 10.90 Oz (309g) GTIN code: 00818905028162 by FreshRealm. Reason: Potential contamination with Listeria monocytogenes.
Details
Source
Food Recall
External ID
H-0180-2026
Action Date
2025-11-19
Status
Terminated
Category
food
Product Description
Loaded Veggie Grain Bowl; Net Wt. 10.90 Oz (309g) GTIN code: 00818905028162
Lot/Code Info: Lot code which is julian date format (YYDDD) 25254 Best by date is 03/10/2026
Quantity Affected: 635 units
Reason for Recall
Potential contamination with Listeria monocytogenes
Distribution
Product was manufactured and shipped direct to consumers in California, Delaware, Florida, Illinois, Indiana, Michigan, New Jersey, New York, Ohio, Pennsylvania, and Texas.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-10-07
Company
San Clemente, CA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 44 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
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 (FreshRealm) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does FreshRealm have FDA actions?
This is the only FDA action we have on record for FreshRealm in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0180-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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