Riclan S.A.
FDA import alert and refusal historyRio Claro, BrazilFEI 3008688090
As of October 25, 2026, Riclan S.A. is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on July 21, 2025, most often for dietary supplement cgmp not met (SUPPL GMP).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Flavored candy, hard (live savers, etc.), without nuts and fruit (without chocolate) · SUPPL GMP
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Riclan S.A.
3 records, newest first. Each line links to the FDA page it came from.
2025
2024
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2017
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
Refusal charges, in plain English
- SUPPL GMP1 refused line
Dietary supplement CGMP not met
The product appeared to be a dietary supplement prepared, packed, or held under conditions that do not meet current good manufacturing practice (CGMP) regulations.
Questions about Riclan S.A.
- Is Riclan S.A. on an FDA import alert?
- No listing for Riclan S.A. appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Brazil page.
- Has FDA refused shipments from Riclan S.A.?
- Yes. FDA refused 1 shipment line from Riclan S.A. on July 21, 2025. The most recent, on July 21, 2025, was flavored candy, hard (live savers, etc.), without nuts and fruit (without chocolate), charged as SUPPL GMP (dietary supplement cgmp not met).
- Why did FDA refuse Riclan S.A.'s shipments?
- The most frequent charge is SUPPL GMP (dietary supplement cgmp not met, 1 line).
- When was Riclan S.A. last inspected by FDA?
- FDA's most recent inspection of Riclan S.A. with a final classification is dated August 8, 2024 and was classified VAI (Voluntary Action Indicated).
- What is Riclan S.A.'s FEI number?
- Riclan S.A.'s FDA Establishment Identifier (FEI) is 3008688090.
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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.