Bralos Fruit SA de CV
FDA import alert and refusal historyUruapan, MexicoFEI 3013779466
Recorded by FDA as BRALOS FRUIT SA DE CV
As of October 27, 2026, Bralos Fruit SA de CV (Uruapan, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for persian limes, published by FDA on February 6, 2018, 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 99-05 · red list
- Last import refusal
- Lime (citrus) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Bralos Fruit SA de CV
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 Bralos Fruit SA de CV
- Is Bralos Fruit SA de CV on an FDA import alert?
- Yes. As of October 27, 2026, Bralos Fruit SA de CV is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for persian limes; FDA published the listing on February 6, 2018.
- Has FDA refused shipments from Bralos Fruit SA de CV?
- Yes. FDA refused 2 shipment lines from Bralos Fruit SA de CV between January 26, 2018 and February 2, 2018. The most recent, on February 2, 2018, was lime (citrus), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Bralos Fruit SA de CV's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Bralos Fruit SA de CV's FEI number?
- Bralos Fruit SA de CV's FDA Establishment Identifier (FEI) is 3013779466.
- Can shipments from Bralos Fruit SA de CV still enter the U.S.?
- Shipments of persian limes from Bralos Fruit SA de CV can be detained without physical examination under Import Alert 99-05; 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.