M.E.Co.,Ltd.
FDA import alert and refusal historyGumi, South KoreaFEI 3018621026
Recorded by FDA as M.E.CO.,LTD.
As of October 25, 2026, M.E.Co.,Ltd. (Gumi, South Korea) is on the red list of FDA Import Alert 99-23 (Produce: contamination with human pathogens) for enoki mushrooms, published by FDA on July 6, 2026, and has 38 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-23 · red list
- Last import refusal
- Enokitake · LISTERIA
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for M.E.Co.,Ltd.
39 records, newest first. Each line links to the FDA page it came from.
2026
- Import alert listingListed on Import Alert 99-23red listEnoki MushroomsSource
2025
2024
- Import refusalSource
Refused, 2 lines in one entry: EnokitakeFSVP VIOEntry E4K-0078280-0Show 2 linesHide lines
- Import refusalSource
Refused, 2 lines in one entry: EnokitakeLISTERIAFSVP VIOEntry E4K-0078349-3Show 2 linesHide lines
- Import refusalRefused, EnokitakeFSVP VIOEntry E4K-0078310-5Source
- Import refusalSource
Refused, 2 lines in one entry: EnokitakeFSVP VIOEntry E4K-0078206-5Show 2 linesHide lines
- Import refusalRefused, EnokitakeFSVP VIOEntry E4K-0078310-5Source
- Import refusalSource
Refused, 2 lines in one entry: EnokitakeLISTERIAFSVP VIOEntry E4K-0078354-3Show 2 linesHide lines
- Import refusalSource
Refused, 2 lines in one entry: EnokitakeFSVP VIOEntry E4K-0078282-6Show 2 linesHide lines
- Import refusalSource
- Import refusalSource
- Import refusalSource
- Import refusalSource
- Import refusalSource
Refused, 2 lines in one entry: EnokitakeFSVP VIOEntry E4K-0078234-7Show 2 linesHide lines
- Import refusalSource
Refused, 2 lines in one entry: EnokitakeFSVP VIOEntry E4K-0078235-4Show 2 linesHide lines
Show 16 earlier records (2022–2024)Hide earlier records
2024
- Import refusalSource
- Import refusalRefused, EnokitakeFSVP VIOEntry E4K-0078262-8Source
- Import refusalSource
- Import refusalRefused, EnokitakeFSVP VIOEntry E4K-0078262-8Source
- Import refusalSource
Refused, 2 lines in one entry: EnokitakeFSVP VIOEntry E4K-0078259-4Show 2 linesHide lines
- Import refusalSource
- Import refusalSource
Refused, 2 lines in one entry: EnokitakeLISTERIAFSVP VIOEntry E4K-0078319-6Show 2 linesHide lines
- Import refusalSource
- Import refusalSource
Refused, 2 lines in one entry: EnokitakeFSVP VIOEntry E4K-0078227-1Show 2 linesHide lines
2023
2022
Refusal charges, in plain English
- FSVP VIO32 refused lines
Importer not in compliance with FSVP
The importer of record appeared not to be in compliance with the Foreign Supplier Verification Program requirements of section 805 of the FD&C Act. The charge concerns the importer's program, not a test result on the food.
- LISTERIA20 refused lines
Listeria monocytogenes
The product appeared to contain Listeria monocytogenes, which the law treats as a poisonous and deleterious substance that may make food injurious to health.
Questions about M.E.Co.,Ltd.
- Is M.E.Co.,Ltd. on an FDA import alert?
- Yes. As of October 25, 2026, M.E.Co.,Ltd. is on the red list of FDA Import Alert 99-23, “Produce: contamination with human pathogens”, for enoki mushrooms; FDA published the listing on July 6, 2026.
- Has FDA refused shipments from M.E.Co.,Ltd.?
- Yes. FDA refused 38 shipment lines from M.E.Co.,Ltd. between October 20, 2022 and February 12, 2025. The most recent, on February 12, 2025, was enokitake, charged as LISTERIA (listeria monocytogenes).
- Why did FDA refuse M.E.Co.,Ltd.'s shipments?
- The most frequent charges are FSVP VIO (importer not in compliance with fsvp, 32 lines) and LISTERIA (listeria monocytogenes, 20 lines).
- What is M.E.Co.,Ltd.'s FEI number?
- M.E.Co.,Ltd.'s FDA Establishment Identifier (FEI) is 3018621026.
- Can shipments from M.E.Co.,Ltd. still enter the U.S.?
- Shipments of enoki mushrooms from M.E.Co.,Ltd. can be detained without physical examination under Import Alert 99-23; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
Buying from M.E.Co.,Ltd.?
Watch it and get the FDA record the day it changes. Free for one supplier.
SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.