Transcafe, S.A.
FDA import alert and refusal historyGuatemala, GuatemalaFEI 3004285246
Recorded by FDA as TRANSCAFE, S.A.
As of October 25, 2026, Transcafe, S.A. is not on any FDA import alert in SupplierRadar's records; FDA refused 4 of its shipment lines on November 25, 2016, most often for pesticide chemical residue (PESTICIDE).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Stringbeans · PESTICIDE
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Transcafe, S.A.
5 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- PESTICIDE4 refused lines
Pesticide chemical residue
The product appeared to contain a pesticide chemical residue that makes it adulterated under section 402(a)(2)(B) of the FD&C Act, for example a residue above the U.S. tolerance or one with no U.S. tolerance for that food.
Questions about Transcafe, S.A.
- Is Transcafe, S.A. on an FDA import alert?
- No listing for Transcafe, 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 Guatemala page.
- Has FDA refused shipments from Transcafe, S.A.?
- Yes. FDA refused 4 shipment lines from Transcafe, S.A. on November 25, 2016. The most recent, on November 25, 2016, was stringbeans, charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Transcafe, S.A.'s shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 4 lines).
- When was Transcafe, S.A. last inspected by FDA?
- FDA's most recent inspection of Transcafe, S.A. with a final classification is dated June 22, 2017 and was classified VAI (Voluntary Action Indicated).
- What is Transcafe, S.A.'s FEI number?
- Transcafe, S.A.'s FDA Establishment Identifier (FEI) is 3004285246.
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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.