Caribe Verde Follajes S.A.
FDA import alert and refusal historySiquirres, Costa RicaFEI 3011289626
As of October 26, 2026, Caribe Verde Follajes S.A. (Siquirres, Costa Rica) is on the red list of FDA Import Alert 99-23 (Produce: contamination with human pathogens) for fresh culantro/ coriander, published by FDA on June 9, 2014, and has no 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
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Caribe Verde Follajes S.A.
2 records, newest first. Each line links to the FDA page it came from.
2015
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
2014
- Import alert listingListed on Import Alert 99-23red listFresh Culantro/ CorianderSource
Questions about Caribe Verde Follajes S.A.
- Is Caribe Verde Follajes S.A. on an FDA import alert?
- Yes. As of October 26, 2026, Caribe Verde Follajes S.A. is on the red list of FDA Import Alert 99-23, “Produce: contamination with human pathogens”, for fresh culantro/ coriander; FDA published the listing on June 9, 2014.
- Has FDA refused shipments from Caribe Verde Follajes S.A.?
- No FDA import refusals for Caribe Verde Follajes S.A. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Caribe Verde Follajes S.A. last inspected by FDA?
- FDA's most recent inspection of Caribe Verde Follajes S.A. with a final classification is dated May 19, 2015 and was classified NAI (No Action Indicated).
- What is Caribe Verde Follajes S.A.'s FEI number?
- Caribe Verde Follajes S.A.'s FDA Establishment Identifier (FEI) is 3011289626.
- Can shipments from Caribe Verde Follajes S.A. still enter the U.S.?
- Shipments of fresh culantro/ coriander from Caribe Verde Follajes S.A. 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.