Irving Franco Rivas
FDA import alert and refusal historyPueblo Santiago Tolman, MexicoFEI 3019742432
Recorded by FDA as IRVING FRANCO RIVAS
As of October 26, 2026, Irving Franco Rivas (Pueblo Santiago Tolman, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for prickly pear, published by FDA on July 12, 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 99-05 · red list
- Last import refusal
- Prickle pear (core fruit) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Irving Franco Rivas
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 Irving Franco Rivas
- Is Irving Franco Rivas on an FDA import alert?
- Yes. As of October 26, 2026, Irving Franco Rivas is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for prickly pear; FDA published the listing on July 12, 2023.
- Has FDA refused shipments from Irving Franco Rivas?
- Yes. FDA refused 2 shipment lines from Irving Franco Rivas between July 7, 2023 and August 10, 2023. The most recent, on August 10, 2023, was prickle pear (core fruit), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Irving Franco Rivas's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Irving Franco Rivas's FEI number?
- Irving Franco Rivas's FDA Establishment Identifier (FEI) is 3019742432.
- Can shipments from Irving Franco Rivas still enter the U.S.?
- Shipments of prickly pear from Irving Franco Rivas 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.