El Paramo
FDA import alert and refusal historyColima, MexicoFEI 3023089208
Recorded by FDA as EL PARAMO
As of October 26, 2026, El Paramo (Colima, Mexico) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for figs, published by FDA on August 6, 2024, and has 1 FDA import refusal 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
- Fig (subtropical and tropical fruit) · PESTICIDE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for El Paramo
2 records, newest first. Each line links to the FDA page it came from.
2024
- Import alert listingListed on Import Alert 99-05red listFigsSource
- Import refusalRefused, Fig (subtropical and tropical fruit)PESTICIDEEntry DR4-0608124-7Source
Refusal charges, in plain English
- PESTICIDE1 refused line
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 El Paramo
- Is El Paramo on an FDA import alert?
- Yes. As of October 26, 2026, El Paramo is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for figs; FDA published the listing on August 6, 2024.
- Has FDA refused shipments from El Paramo?
- Yes. FDA refused 1 shipment line from El Paramo on June 28, 2024. The most recent, on June 28, 2024, was fig (subtropical and tropical fruit), charged as PESTICIDE (pesticide chemical residue).
- Why did FDA refuse El Paramo's shipments?
- The most frequent charge is PESTICIDE (pesticide chemical residue, 1 line).
- What is El Paramo's FEI number?
- El Paramo's FDA Establishment Identifier (FEI) is 3023089208.
- Can shipments from El Paramo still enter the U.S.?
- Shipments of figs from El Paramo 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.