Profrutas Cia, Ltda
FDA import alert and refusal historyGuayaquil, EcuadorFEI 3016493502
Recorded by FDA as PROFRUTAS CIA, LTDA
As of October 27, 2026, Profrutas Cia, Ltda (Guayaquil, Ecuador) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for blackberries, published by FDA on November 21, 2022, and has 2 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-08 · red list
- Last import refusal
- Blackberries (berry) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Profrutas Cia, Ltda
3 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- PESTICIDE2 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 Profrutas Cia, Ltda
- Is Profrutas Cia, Ltda on an FDA import alert?
- Yes. As of October 27, 2026, Profrutas Cia, Ltda is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for blackberries; FDA published the listing on November 21, 2022.
- Has FDA refused shipments from Profrutas Cia, Ltda?
- Yes. FDA refused 2 shipment lines from Profrutas Cia, Ltda between December 6, 2022 and July 28, 2025. The most recent, on July 28, 2025, was blackberries (berry), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Profrutas Cia, Ltda's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Profrutas Cia, Ltda's FEI number?
- Profrutas Cia, Ltda's FDA Establishment Identifier (FEI) is 3016493502.
- Can shipments from Profrutas Cia, Ltda still enter the U.S.?
- Shipments of blackberries from Profrutas Cia, Ltda can be detained without physical examination under Import Alert 99-08; 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.