Tomas Franco Beltran
FDA import alert and refusal historyOtumba, MexicoFEI 3027559831
Recorded by FDA as TOMAS FRANCO BELTRAN
As of October 26, 2026, Tomas Franco Beltran (Otumba, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for prickle pear, published by FDA on September 25, 2024, 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
- Prickle pear (core fruit) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Tomas Franco Beltran
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 Tomas Franco Beltran
- Is Tomas Franco Beltran on an FDA import alert?
- Yes. As of October 26, 2026, Tomas Franco Beltran is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for prickle pear; FDA published the listing on September 25, 2024.
- Has FDA refused shipments from Tomas Franco Beltran?
- Yes. FDA refused 2 shipment lines from Tomas Franco Beltran between September 18, 2024 and October 1, 2024. The most recent, on October 1, 2024, was prickle pear (core fruit), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Tomas Franco Beltran's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Tomas Franco Beltran's FEI number?
- Tomas Franco Beltran's FDA Establishment Identifier (FEI) is 3027559831.
- Can shipments from Tomas Franco Beltran still enter the U.S.?
- Shipments of prickle pear from Tomas Franco Beltran 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.