DR. AG Co., Ltd.
FDA import alert and refusal historyCheongdo, South KoreaFEI 3011403788
As of October 26, 2026, DR. AG Co., Ltd. (Cheongdo, 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 August 11, 2020, and has 6 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 mushrooms, whole (button) (fungi) · LISTERIA
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for DR. AG Co., Ltd.
8 records, newest first. Each line links to the FDA page it came from.
2022
2021
2020
- Import refusalSource
Refused, 2 lines in one entry: Enokitake mushrooms, whole (button) (fungi)POISONOUSEntry AWJ-0210534-9Show 2 linesHide lines
- Import alert listingListed on Import Alert 99-23red listEnoki MushroomsSource
2017
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
Refusal charges, in plain English
- POISONOUS4 refused lines
Poisonous or deleterious substance
The product appeared to bear or contain a poisonous or deleterious substance which may render it injurious to health.
- LISTERIA3 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.
- MFR INSAN3 refused lines
Insanitary manufacturing, processing or packing
The product appeared to have been manufactured, processed, or packed under insanitary conditions, which is a ground for refusal under section 801(a)(1) of the FD&C Act.
- MFR INJ1 refused line
Insanitary conditions, may be injurious
The product appeared to have been prepared, packed, or held under insanitary conditions whereby it may have been rendered injurious to health.
Questions about DR. AG Co., Ltd.
- Is DR. AG Co., Ltd. on an FDA import alert?
- Yes. As of October 26, 2026, DR. AG 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 August 11, 2020.
- Has FDA refused shipments from DR. AG Co., Ltd.?
- Yes. FDA refused 6 shipment lines from DR. AG Co., Ltd. between November 5, 2020 and March 16, 2022. The most recent, on March 16, 2022, was enokitake mushrooms, whole (button) (fungi), charged as LISTERIA (listeria monocytogenes).
- Why did FDA refuse DR. AG Co., Ltd.'s shipments?
- The most frequent charges are POISONOUS (poisonous or deleterious substance, 4 lines) and LISTERIA (listeria monocytogenes, 3 lines).
- When was DR. AG Co., Ltd. last inspected by FDA?
- FDA's most recent inspection of DR. AG Co., Ltd. with a final classification is dated September 25, 2017 and was classified VAI (Voluntary Action Indicated).
- What is DR. AG Co., Ltd.'s FEI number?
- DR. AG Co., Ltd.'s FDA Establishment Identifier (FEI) is 3011403788.
- Can shipments from DR. AG Co., Ltd. still enter the U.S.?
- Shipments of enoki mushrooms from DR. AG 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).
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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.