Grupo Frutexport, S.A.
FDA import alert and refusal historyZamora, MexicoFEI 3013208086
Recorded by FDA as GRUPO FRUTEXPORT, S.A.
As of October 26, 2026, Grupo Frutexport, S.A. (Zamora, Mexico) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for frozen strawberries, published by FDA on April 14, 2017, 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
- Strawberries (berry) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Grupo Frutexport, S.A.
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 Grupo Frutexport, S.A.
- Is Grupo Frutexport, S.A. on an FDA import alert?
- Yes. As of October 26, 2026, Grupo Frutexport, S.A. is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for frozen strawberries; FDA published the listing on April 14, 2017.
- Has FDA refused shipments from Grupo Frutexport, S.A.?
- Yes. FDA refused 2 shipment lines from Grupo Frutexport, S.A. between March 16, 2017 and March 8, 2019. The most recent, on March 8, 2019, was strawberries (berry), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Grupo Frutexport, S.A.'s shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Grupo Frutexport, S.A.'s FEI number?
- Grupo Frutexport, S.A.'s FDA Establishment Identifier (FEI) is 3013208086.
- Can shipments from Grupo Frutexport, S.A. still enter the U.S.?
- Shipments of frozen strawberries from Grupo Frutexport, S.A. 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.