RE&S Japan
FDA import alert and refusal historyOsaka, JapanFEI 3014793755
As of October 26, 2026, RE&S Japan is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines between November 29, 2022 and March 10, 2023, most often for fd&c yellow no. 5 not declared (YELLOW #5).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Radish (root & tuber vegetable) · YELLOW #5
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for RE&S Japan
4 records, newest first. Each line links to the FDA page it came from.
2025
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2023
2022
- Import refusalRefused, Radish (root & tuber vegetable)UNSAFE COLYELLOW #5Entry EVJ-1179944-5Source
- Import refusalRefused, Radish (root & tuber vegetable)UNSAFE COLYELLOW #5Entry EVJ-1179695-3Source
Refusal charges, in plain English
- YELLOW #53 refused lines
FD&C Yellow No. 5 not declared
The food appeared to contain the color additive FD&C Yellow No. 5 without declaring it on the label as 21 CFR 74.705 requires.
- UNSAFE COL2 refused lines
Color additive unsafe under section 721
The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.
Questions about RE&S Japan
- Is RE&S Japan on an FDA import alert?
- No listing for RE&S Japan appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Japan page.
- Has FDA refused shipments from RE&S Japan?
- Yes. FDA refused 3 shipment lines from RE&S Japan between November 29, 2022 and March 10, 2023. The most recent, on March 10, 2023, was radish (root & tuber vegetable), charged as YELLOW #5 (fd&c yellow no. 5 not declared).
- Why did FDA refuse RE&S Japan's shipments?
- The most frequent charges are YELLOW #5 (fd&c yellow no. 5 not declared, 3 lines) and UNSAFE COL (color additive unsafe under section 721, 2 lines).
- When was RE&S Japan last inspected by FDA?
- FDA's most recent inspection of RE&S Japan with a final classification is dated October 29, 2025 and was classified VAI (Voluntary Action Indicated).
- What is RE&S Japan's FEI number?
- RE&S Japan's FDA Establishment Identifier (FEI) is 3014793755.
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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.