Raymundo Solis Juarez
FDA import alert and refusal historyAcatzingo, MexicoFEI 3011459631
As of October 26, 2026, Raymundo Solis Juarez (Acatzingo, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for yellow prickly pear (tuna amarilla), published by FDA on July 9, 2025, 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 Raymundo Solis Juarez
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 Raymundo Solis Juarez
- Is Raymundo Solis Juarez on an FDA import alert?
- Yes. As of October 26, 2026, Raymundo Solis Juarez is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for yellow prickly pear (tuna amarilla); FDA published the listing on July 9, 2025.
- Has FDA refused shipments from Raymundo Solis Juarez?
- Yes. FDA refused 2 shipment lines from Raymundo Solis Juarez between June 16, 2025 and August 15, 2025. The most recent, on August 15, 2025, was prickle pear (core fruit), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Raymundo Solis Juarez's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Raymundo Solis Juarez's FEI number?
- Raymundo Solis Juarez's FDA Establishment Identifier (FEI) is 3011459631.
- Can shipments from Raymundo Solis Juarez still enter the U.S.?
- Shipments of yellow prickly pear (tuna amarilla) from Raymundo Solis Juarez 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.