FDA Recall United States Terminated Historical recordClass I
Forest Mushroom Food Inc.
- Product
- Guan's Enoki Mushroom; Champignon d'enoki 100 g/3.5 oz. and…
- Published
- May 26, 2021
- Distribution
- Nationwide
Public Health Trace republishes official recall, outbreak, and surveillance data from CDC, FDA, USDA, WHO, and other public sources. It is an independent information service, not a medical provider, and not a substitute for professional medical advice or your local public health department's own guidance.
Please review the following before continuing:
Policy version 2026-07-21, effective July 21, 2026.
United States
TerminatedClass I
California Department of Public Health collected samples at retail and found Listeria monocytogenes in Enoki mushrooms from Korea
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Guan's Enoki Mushrooms; Net Weight 200 g - 7.05 oz. UPC: 8 59267007013 Product Number:50130 Product of Korea, Keep refrigerated Distributed by Guan's Mushroom Co. Los Angeles, CA Package is clear plastic top with Guan's logo, green bottom with Enoki Mushroom in English, Korean and French | Not published in this source record | 2479 boxes (25 individual packages per box) | Package Code 14 1; ID# 01357801; Lot number: 01357801 Use by date: 2020-03-18 |
Responsible company: Forest Mushroom Food Inc.
FDA Recall United States Terminated Historical recordClass I
FDA Recall United States Terminated Historical recordClass I
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.
| State | Distributed |
|---|---|
| Hawaii | 1 |
| California | 1 |
| Washington | 1 |
| Georgia | 1 |
| Florida | 1 |
| Minnesota | 1 |
| Michigan | 1 |
| Illinois | 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.
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
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.
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.