RecallHawk
Class I Recall

BLACK AND WHITE GLUTINOUS RICE BALLS WITH BLACK SESAME FILLING NET WT. 14.1 OZ (400 g) Product of China UPC: 69087910000

KHONG GUAN (HQ)

Summary

The FDA issued a Class I for BLACK AND WHITE GLUTINOUS RICE BALLS WITH BLACK SESAME FILLING NET WT. 14.1 OZ ( by KHONG GUAN (HQ). Reason: Undeclared peanuts..

Details

Source

Food Recall

External ID

H-1260-2026

Action Date

2026-09-02

Status

Ongoing

Category

food

Product Description

BLACK AND WHITE GLUTINOUS RICE BALLS WITH BLACK SESAME FILLING NET WT. 14.1 OZ (400 g) Product of China UPC: 6908791000084

Lot/Code Info: USE BY: 10/19/2027

Quantity Affected: 37 cases (33 units/case)

Reason for Recall

Undeclared peanuts.

Distribution

Domestic: AZ, CA, CO, HI, NJ, OR, TX, WA. Foreign: Not applicable.

Type: Voluntary: Firm initiated

Recall Initiated: 2026-07-13

Company

KHONG GUAN (HQ)

Union City, 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 47 food recalls issued in the same week, part of 82 food-related FDA actions this month.

KHONG GUAN (HQ) has 2 FDA actions in our database, including 2 recalls.

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 (KHONG GUAN (HQ)) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does KHONG GUAN (HQ) have FDA actions?

KHONG GUAN (HQ) 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-1260-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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