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Disclaimer: Recall Radar is an informational summary of public FDA enforcement reports. It is not medical advice. Always confirm details with the FDA, the company, a pharmacist, or a doctor before making health decisions.

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Class IFood

Glutinous Rice Balls with Black Sesame Filling recall

Summary

KHONG GUAN (HQ) is recalling Glutinous Rice Balls with Black Sesame Filling NET WT. 14.1 OZ (400 g) Product o… (food). According to the FDA report, the reason is: Undeclared peanuts. The FDA rated this a Class I: most serious: there is a reasonable chance the product could cause serious health problems or death. Recall status: Ongoing.

Understanding this recall

What happened

Khong Guan is recalling Glutinous Rice Balls with Black Sesame Filling because it contains peanuts that aren't declared on the label.

Why it matters

Peanut is one of the major food allergens. For people with a peanut allergy, even a small amount can cause a reaction ranging from hives and swelling to anaphylaxis, which is life-threatening. If peanut isn't on the label, an allergic person has no warning.

Who should pay attention

People with peanut allergies in AZ, CA, CO, HI, NJ, OR, TX and WA.
Distribution in the FDA report: Domestic: AZ, CA, CO, HI, NJ, OR, TX, WA. Foreign: Not applicable.

How to check your product

Check the use-by date on the package.
Codes listed by the FDA: USE BY: 10/19/2027; 9/22/2027

Based only on the FDA enforcement record plus general public-health background on this type of hazard. Not medical advice; if you have symptoms or concerns, contact a doctor or pharmacist.

Details from the FDA report

Product
Glutinous Rice Balls with Black Sesame Filling NET WT. 14.1 OZ (400 g) Product of China UPC: 6908791000053
Reason
Undeclared peanuts.
Lot / code info
USE BY: 10/19/2027; 9/22/2027
Quantity
87 cases (36 units/case)
Distribution
Domestic: AZ, CA, CO, HI, NJ, OR, TX, WA. Foreign: Not applicable.
Recalling company
KHONG GUAN (HQ), Union City, CA United States
Recall started
July 13, 2026
FDA report date
September 2, 2026
Classification
Class I: Most serious: there is a reasonable chance the product could cause serious health problems or death.
Voluntary / mandated
Voluntary: Firm initiated
Status
Ongoing
Recall number
H-1259-2026

What to do

View the FDA source record (openFDA) · FDA recalls page

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