Sucos Do Brasil S/A
FDA import alert and refusal historyPacajus, BrazilFEI 3005168470
As of October 26, 2026, Sucos Do Brasil S/A (Pacajus, Brazil) is on the red list of FDA Import Alert 99-21 (Foods with undeclared added sulfiting agents) for acerola juice, published by FDA on October 23, 2019, is also listed on Import Alert 99-39 (red list), 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 99-21 · red listIA 99-39 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Sucos Do Brasil S/A
3 records, newest first. Each line links to the FDA page it came from.
2019
- Import alert listingListed on Import Alert 99-21red listAcerola JuiceSource
2015
- Import alert listingListed on Import Alert 99-39red listAcerola JuiceSource
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
Questions about Sucos Do Brasil S/A
- Is Sucos Do Brasil S/A on an FDA import alert?
- Yes. As of October 26, 2026, Sucos Do Brasil S/A is on the red list of FDA Import Alert 99-21, “Foods with undeclared added sulfiting agents”, for acerola juice; FDA published the listing on October 23, 2019.
- Has FDA refused shipments from Sucos Do Brasil S/A?
- No FDA import refusals for Sucos Do Brasil S/A appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Sucos Do Brasil S/A last inspected by FDA?
- FDA's most recent inspection of Sucos Do Brasil S/A with a final classification is dated March 5, 2015 and was classified VAI (Voluntary Action Indicated).
- What is Sucos Do Brasil S/A's FEI number?
- Sucos Do Brasil S/A's FDA Establishment Identifier (FEI) is 3005168470.
- Can shipments from Sucos Do Brasil S/A still enter the U.S.?
- Shipments of acerola juice from Sucos Do Brasil S/A can be detained without physical examination under Import Alert 99-21; 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.