H.A.Co.,Ltd.
FDA import alert and refusal historyCheongdo, South KoreaFEI 3027471573
Recorded by FDA as H.A.CO.,LTD.
As of October 26, 2026, H.A.Co.,Ltd. is on the green list of FDA Import Alert 25-21, which exempts its listed products from detention without physical examination under that alert, and has 4 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 25-21 · green list
- Last import refusal
- Enokitake · LISTERIA
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for H.A.Co.,Ltd.
5 records, newest first. Each line links to the FDA page it came from.
2025
- Import refusalSource
Refused, 2 lines in one entry: EnokitakeLISTERIAEntry EJA-5210161-7Show 2 linesHide lines
- Import refusalSource
Refused, 2 lines in one entry: EnokitakeLISTERIAEntry EJA-5209422-6Show 2 linesHide lines
- Import alert listingListed on Import Alert 25-21green listEnoki MushroomSource
Refusal charges, in plain English
- LISTERIA4 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 H.A.Co.,Ltd.
- Is H.A.Co.,Ltd. on an FDA import alert?
- Yes. As of October 26, 2026, H.A.Co.,Ltd. is on the green list of FDA Import Alert 25-21, “Enoki mushrooms from Korea and China: Listeria”, for enoki mushroom; FDA published the listing on April 4, 2025.
- Has FDA refused shipments from H.A.Co.,Ltd.?
- Yes. FDA refused 4 shipment lines from H.A.Co.,Ltd. between April 9, 2025 and May 27, 2025. The most recent, on May 27, 2025, was enokitake, charged as LISTERIA (listeria monocytogenes).
- Why did FDA refuse H.A.Co.,Ltd.'s shipments?
- The most frequent charge is LISTERIA (listeria monocytogenes, 4 lines).
- What is H.A.Co.,Ltd.'s FEI number?
- H.A.Co.,Ltd.'s FDA Establishment Identifier (FEI) is 3027471573.
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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.