Eric Carpio Juarez
FDA import alert and refusal historyAcatzingo, MexicoFEI 3024216705
Recorded by FDA as ERIC CARPIO JUAREZ
As of October 25, 2026, Eric Carpio Juarez (Acatzingo, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for hawthorn; tejocote, published by FDA on November 15, 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
- Haw · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Eric Carpio 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 Eric Carpio Juarez
- Is Eric Carpio Juarez on an FDA import alert?
- Yes. As of October 25, 2026, Eric Carpio Juarez is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for hawthorn; tejocote; FDA published the listing on November 15, 2024.
- Has FDA refused shipments from Eric Carpio Juarez?
- Yes. FDA refused 2 shipment lines from Eric Carpio Juarez between November 8, 2024 and December 23, 2024. The most recent, on December 23, 2024, was haw, charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Eric Carpio Juarez's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Eric Carpio Juarez's FEI number?
- Eric Carpio Juarez's FDA Establishment Identifier (FEI) is 3024216705.
- Can shipments from Eric Carpio Juarez still enter the U.S.?
- Shipments of hawthorn; tejocote from Eric Carpio 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.