J Jesus Espinoza Bravo
FDA import alert and refusal historyTaretan, MexicoFEI 3016425924
Recorded by FDA as J JESUS ESPINOZA BRAVO
As of October 26, 2026, J Jesus Espinoza Bravo (Taretan, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for guava, published by FDA on July 9, 2026, 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
- Guava (subtropical and tropical fruit) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for J Jesus Espinoza Bravo
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 J Jesus Espinoza Bravo
- Is J Jesus Espinoza Bravo on an FDA import alert?
- Yes. As of October 26, 2026, J Jesus Espinoza Bravo is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for guava; FDA published the listing on July 9, 2026.
- Has FDA refused shipments from J Jesus Espinoza Bravo?
- Yes. FDA refused 2 shipment lines from J Jesus Espinoza Bravo between July 1, 2026 and July 6, 2026. The most recent, on July 6, 2026, was guava (subtropical and tropical fruit), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse J Jesus Espinoza Bravo's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is J Jesus Espinoza Bravo's FEI number?
- J Jesus Espinoza Bravo's FDA Establishment Identifier (FEI) is 3016425924.
- Can shipments from J Jesus Espinoza Bravo still enter the U.S.?
- Shipments of guava from J Jesus Espinoza Bravo 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.