LUNDBERG FAMILY FAMRS WHITE RICE JASMINE NET WT 32 OZ (2 lb) 907 g Manufactured and Distributed by: Lundberg Family Far
Summary
The FDA issued a Class II for LUNDBERG FAMILY FAMRS WHITE RICE JASMINE NET WT 32 OZ (2 lb) 907 g Manufactured by Wehah Farms. Reason: Potential contamination with foreign materials..
Details
Source
Food Recall
External ID
H-0767-2026
Action Date
2026-05-13
Status
Ongoing
Category
food
Product Description
LUNDBERG FAMILY FAMRS WHITE RICE JASMINE NET WT 32 OZ (2 lb) 907 g Manufactured and Distributed by: Lundberg Family Farms Richvale, CA 95974 UPC: 073416040281
Lot/Code Info: Lot, Best Before: 260201MA, 01FEB2027; 260202MA, 02FEB2027.
Quantity Affected: 27,324 packages (6 packages/case; 4,554 cases)
Reason for Recall
Potential contamination with foreign materials.
Distribution
U.S. States: CA, CT, FL, IL, NC, NH, NY, PA, TN, VT, WA, WI. Foreign distribution: None
Type: Voluntary: Firm initiated
Recall Initiated: 2026-04-03
Company
Richvale, 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 93 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Wehah Farms has 2 FDA actions in our database, including 2 recalls.
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 (Wehah Farms) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Wehah Farms have FDA actions?
Wehah Farms 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 "H-0767-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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