Ruben Bigurra Proom
FDA import alert and refusal historyMartinez De La Torre, MexicoFEI 3025477027
Recorded by FDA as RUBEN BIGURRA PROOM
As of October 26, 2026, Ruben Bigurra Proom (Martinez De La Torre, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for lime, published by FDA on April 6, 2026, and has 3 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 Ruben Bigurra Proom
4 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- PESTICIDE3 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 Ruben Bigurra Proom
- Is Ruben Bigurra Proom on an FDA import alert?
- Yes. As of October 26, 2026, Ruben Bigurra Proom is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for lime; FDA published the listing on April 6, 2026.
- Has FDA refused shipments from Ruben Bigurra Proom?
- Yes. FDA refused 3 shipment lines from Ruben Bigurra Proom between March 23, 2026 and March 24, 2026. The most recent, on March 24, 2026, was lime (citrus), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Ruben Bigurra Proom's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 3 lines).
- What is Ruben Bigurra Proom's FEI number?
- Ruben Bigurra Proom's FDA Establishment Identifier (FEI) is 3025477027.
- Can shipments from Ruben Bigurra Proom still enter the U.S.?
- Shipments of lime from Ruben Bigurra Proom 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.