FDA Recall United States TerminatedTerminated: February 17, 2022Historical 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
Forest Mushroom Food Inc. Recall: California Department of Public Health collected samples at retail and found Listeria monocytogenes in Enoki mushrooms from Korea - F-0910-2020
United States
TerminatedClass I
- Company
- Forest Mushroom Food Inc.
- Product
- Guan's Enoki Mushrooms; Net Weight 200 g - 7.05 oz. UPC: 8…
- Recall date
- March 11, 2020
- Terminated
- March 19, 2021
- Source
- FDA
Reason for recall
California Department of Public Health collected samples at retail and found Listeria monocytogenes in Enoki mushrooms from Korea
- - Recall initiated
- - Reported by source
- - Recall terminated
| 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 |
Distribution
- HI
- CA
- WA
- GA
- FL
- MN
- MI
- IL
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0910-2020
- Event ID
- 85291
- Status
- Terminated
- Classification
- Class I
- Company
- Forest Mushroom Food Inc.
- Product description
- 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
- Quantity
- 2479 boxes (25 individual packages per box)
- Reason
- California Department of Public Health collected samples at retail and found Listeria monocytogenes in Enoki mushrooms from Korea
- Recall initiation date
- March 11, 2020
- Report date
- April 8, 2020
- Classification date
- Not published in this source record
- Termination date
- March 19, 2021
- Distribution pattern
- HI, CA, WA, GA, FL, MN, MI, IL,
- UPC, lot, and code information
- Package Code 14 1; ID# 01357801; Lot number: 01357801 Use by date: 2020-03-18
- 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: Forest Mushroom Food Inc.
Other recalls from Forest Mushroom Food Inc.
FDA Recall United States TerminatedTerminated: February 18, 2022Historical recordClass I
Forest Mushroom Food Inc.
- Product
- Guan's Enoki Mushroom - Champigons d'enoki; Net Wt./ Poids…
- Published
- May 12, 2021
- Distribution
- Nationwide
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.
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. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.
New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.
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 I mean?
FDA classifies this recall as Class I. See how to read an FDA recall record (linked above) for what each classification level means.
Is this recall still active?
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.
What should I do if I have this product?
Follow the responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.
Official guidance and record verification
Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.
How to interpret this historical record
This record is preserved as published by FDA, as of March 19, 2021.
Status as reported: Terminated.
This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.
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.