Jbr
FDA import alert and refusal historyTongyeong, South KoreaFEI 3029914863
Recorded by FDA as JBR
As of October 26, 2026, Jbr (Tongyeong, South Korea) is on the red list of FDA Import Alert 16-50 (Molluscan bivalve shellfish) for all fresh and frozen bivalve molluscan shellfish products, published by FDA on September 2, 2025, is also listed on Import Alert 16-137 (red list), and has 8 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 16-50 · red listIA 16-137 · red list
- Last import refusal
- Oysters · POISONOUS
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Jbr
10 records, newest first. Each line links to the FDA page it came from.
2025
- Import refusalSource
Refused, 2 lines in one entry: OystersPOISONOUSINSANITARYEntry EJA-5217393-9Show 2 linesHide lines
- Refused, OystersPOISONOUSINSANITARYEntry EJA-5217393-9Source
- Refused, OystersPOISONOUSINSANITARYEntry EJA-5217393-9Source
- Import refusalSource
Refused, 3 lines in one entry: OystersPOISONOUSINSANITARYEntry EJA-5217178-4Show 3 linesHide lines
- Refused, OystersPOISONOUSINSANITARYEntry EJA-5217178-4Source
- Refused, OystersPOISONOUSINSANITARYEntry EJA-5217178-4Source
- Refused, OystersPOISONOUSINSANITARYEntry EJA-5217178-4Source
- Import refusalSource
Refused, 2 lines in one entry: OystersPOISONOUSINSANITARYMFR INSANEntry EJA-5216955-6Show 2 linesHide lines
- Refused, OystersPOISONOUSINSANITARYMFR INSANEntry EJA-5216955-6Source
- Refused, OystersPOISONOUSINSANITARYMFR INSANEntry EJA-5216955-6Source
- Import alert listingListed on Import Alert 16-50red listAll fresh and frozen bivalve molluscan shellfish productsSource
2024
- Import alert listingListed on Import Alert 16-137red listOysters RockefellerSource
- Import refusalRefused, Oysters, aquaculture harvested fishery/seafood productsPOISONOUSINCONSPICUFALSEINSANITARYEntry ASW-0164204-9Source
Refusal charges, in plain English
- INSANITARY8 refused lines
Prepared, packed or held under insanitary conditions
The product appeared to have been prepared, packed, or held under insanitary conditions whereby it may have been contaminated with filth or rendered injurious to health.
- POISONOUS8 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.
- MFR INSAN2 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.
- FALSE1 refused line
False or misleading labeling
The labeling appeared to be false or misleading in some particular.
- INCONSPICU1 refused line
Required information not conspicuous
Information required on the label appeared not to be placed prominently or conspicuously enough to be read and understood by an ordinary consumer.
Questions about Jbr
- Is Jbr on an FDA import alert?
- Yes. As of October 26, 2026, Jbr is on the red list of FDA Import Alert 16-50, “Molluscan bivalve shellfish”, for all fresh and frozen bivalve molluscan shellfish products; FDA published the listing on September 2, 2025.
- Has FDA refused shipments from Jbr?
- Yes. FDA refused 8 shipment lines from Jbr between August 19, 2024 and November 4, 2025. The most recent, on November 4, 2025, was oysters, charged as POISONOUS (poisonous or deleterious substance).
- Why did FDA refuse Jbr's shipments?
- The most frequent charges are INSANITARY (prepared, packed or held under insanitary conditions, 8 lines) and POISONOUS (poisonous or deleterious substance, 8 lines).
- What is Jbr's FEI number?
- Jbr's FDA Establishment Identifier (FEI) is 3029914863.
- Can shipments from Jbr still enter the U.S.?
- Shipments of all fresh and frozen bivalve molluscan shellfish products from Jbr can be detained without physical examination under Import Alert 16-50; 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.