Listo y Fresco
FDA import alert and refusal historyCali, ColombiaFEI 3004251363
As of October 26, 2026, Listo y Fresco (Cali, Colombia) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for blackberries, published by FDA on April 14, 2023, 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 Listo y Fresco
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 Listo y Fresco
- Is Listo y Fresco on an FDA import alert?
- Yes. As of October 26, 2026, Listo y Fresco is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for blackberries; FDA published the listing on April 14, 2023.
- Has FDA refused shipments from Listo y Fresco?
- Yes. FDA refused 2 shipment lines from Listo y Fresco between May 12, 2023 and September 20, 2023. The most recent, on September 20, 2023, was blackberries (berry), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Listo y Fresco's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Listo y Fresco's FEI number?
- Listo y Fresco's FDA Establishment Identifier (FEI) is 3004251363.
- Can shipments from Listo y Fresco still enter the U.S.?
- Shipments of blackberries from Listo y Fresco 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.