Edwin Mendoza Solis
FDA import alert and refusal historyManagua, NicaraguaFEI 3013248963
As of October 26, 2026, Edwin Mendoza Solis (Managua, Nicaragua) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for dasheen (taro/yautia), published by FDA on April 24, 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
- Taro, dasheen (root & tuber vegetable) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Edwin Mendoza Solis
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 Edwin Mendoza Solis
- Is Edwin Mendoza Solis on an FDA import alert?
- Yes. As of October 26, 2026, Edwin Mendoza Solis is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for dasheen (taro/yautia); FDA published the listing on April 24, 2025.
- Has FDA refused shipments from Edwin Mendoza Solis?
- Yes. FDA refused 2 shipment lines from Edwin Mendoza Solis between April 23, 2025 and April 28, 2025. The most recent, on April 28, 2025, was taro, dasheen (root & tuber vegetable), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse Edwin Mendoza Solis's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 2 lines).
- What is Edwin Mendoza Solis's FEI number?
- Edwin Mendoza Solis's FDA Establishment Identifier (FEI) is 3013248963.
- Can shipments from Edwin Mendoza Solis still enter the U.S.?
- Shipments of dasheen (taro/yautia) from Edwin Mendoza Solis 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.