Has FDA refused shipments from Bada Myeongga?

Yes. FDA refused 5 shipment lines from Bada Myeongga between April 23, 2025 and December 22, 2025. The most recent, on December 22, 2025, was seaweed, dried or paste, charged as POISONOUS (poisonous or deleterious substance).

Why did FDA refuse Bada Myeongga's shipments?

The most frequent charges are POISONOUS (poisonous or deleterious substance, 4 lines) and POISONORD (poisonous or deleterious substance (ordinarily injurious), 1 line).

What is Bada Myeongga's FEI number?

Bada Myeongga's FDA Establishment Identifier (FEI) is 3011391152.

Can shipments from Bada Myeongga still enter the U.S.?

Shipments of dried sea mustard (seaweed) from Bada Myeongga can be detained without physical examination under Import Alert 99-42; 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).

Bada Myeongga

FDA import alert and refusal historyWando, South KoreaFEI 3011391152

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As of October 25, 2026, Bada Myeongga (Wando, South Korea) is on the red list of FDA Import Alert 99-42 (Foods: heavy metal (toxic element) contamination) for dried sea mustard (seaweed), published by FDA on April 21, 2025, and has 5 FDA import refusals recorded since October 2016.

Data from FDA public records, last checked October 25, 2026. Request a correction

Current status

Import alerts: IA 99-42 · red list
Last import refusal: Dec 22, 2025Seaweed, dried or paste · POISONOUS
Last warning letter: None found
Last inspection: None on record

Every FDA record for Bada Myeongga

6 records, newest first. Each line links to the FDA page it came from.

2025

Dec 22, 2025Import refusal
Refused, Seaweed, dried or pastePOISONOUSEntry NQA-0001436-2
Source
Dec 22, 2025Import refusal
Refused, Seaweed, dried or pastePOISONOUSEntry U47-2506562-5
Source
Jul 10, 2025Import refusal
Refused, Seaweed, dried or pastePOISONOUSEntry NQA-0000521-2
Source
Apr 23, 2025Import refusal
Refused, 2 lines in one entry: Seaweed, dried or pastePOISONORDPOISONOUSEntry EKY-2412170-2Show 2 linesHide lines
- Refused, Seaweed, dried or pastePOISONORDEntry EKY-2412170-2Source
- Refused, Seaweed, dried or pastePOISONOUSEntry EKY-2412170-2Source
Source
Apr 21, 2025Import alert listing
Listed on Import Alert 99-42red listDried Sea Mustard (SeaWeed)
Source

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.
POISONORD1 refused line
Poisonous or deleterious substance (ordinarily injurious)
The product appeared to contain a poisonous or deleterious substance in a form or amount that would ordinarily render it injurious to health.

Questions about Bada Myeongga

Is Bada Myeongga on an FDA import alert?: Yes. As of October 25, 2026, Bada Myeongga is on the red list of FDA Import Alert 99-42, “Foods: heavy metal (toxic element) contamination”, for dried sea mustard (seaweed); FDA published the listing on April 21, 2025.
Has FDA refused shipments from Bada Myeongga?: Yes. FDA refused 5 shipment lines from Bada Myeongga between April 23, 2025 and December 22, 2025. The most recent, on December 22, 2025, was seaweed, dried or paste, charged as POISONOUS (poisonous or deleterious substance).
Why did FDA refuse Bada Myeongga's shipments?: The most frequent charges are POISONOUS (poisonous or deleterious substance, 4 lines) and POISONORD (poisonous or deleterious substance (ordinarily injurious), 1 line).
What is Bada Myeongga's FEI number?: Bada Myeongga's FDA Establishment Identifier (FEI) is 3011391152.
Can shipments from Bada Myeongga still enter the U.S.?: Shipments of dried sea mustard (seaweed) from Bada Myeongga can be detained without physical examination under Import Alert 99-42; 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.