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Kwok Shing, Inc. Recall: Potential contamination with pesticides.

United States

OngoingClass III

Company
Kwok Shing, Inc.
Product
American Ginsengs. PRODUCT OF WISCONSIN. NET WT: 4 oz. NET W…
Recall date
September 8, 2026
Source
FDA

Reason for recall

Potential contamination with pesticides.

  1. - Recall initiated
  2. - Reported by source
Recalled products
Product description UPC Quantity Lot / code information
American Ginsengs. PRODUCT OF WISCONSIN. NET WT: 4 oz. NET WT. 8 oz. Not published in this source record 70 boxes 108-728-420

Distribution

  • Domestic: CA. Foreign: Not Applicable.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
H-1393-2026
Event ID
99859
Status
Ongoing
Classification
Class III
Company
Kwok Shing, Inc.
Product description
American Ginsengs. PRODUCT OF WISCONSIN. NET WT: 4 oz. NET WT. 8 oz.
Quantity
70 boxes
Reason
Potential contamination with pesticides.
Recall initiation date
September 8, 2026
Report date
September 30, 2026
Classification date
Not published in this source record
Termination date
Not terminated as of this source record
Distribution pattern
Domestic: CA. Foreign: Not Applicable.
UPC, lot, and code information
108-728-420
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Letter
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Kwok Shing, Inc.

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
California 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class III mean?

A situation in which use of or exposure to a product is not likely to cause adverse health consequences.

Is this recall still active?

According to FDA, this recall's status is "Ongoing." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.